Name: rs59581806
Published: September 21, 2022
License: Open Access

Welcome to the Reference SNP (rs) Report

All alleles are reported in the Forward orientation. Click on the Variant Details tab for details on Genomic Placement, Gene, and Amino Acid changes. HGVS names are in the HGVS tab.

Reference SNP (rs) Report

This page reports data for a single dbSNP Reference SNP variation (RefSNP or rs) from the new redesigned dbSNP build.
Top of the page reports a concise summary for the rs, with more specific details included in the corresponding tabs below.
All alleles are reported in the Forward orientation. Use the Genomic View to inspect the nucleotides flanking the variant, and its neighbors.
For more information see Help documentation.

rs59581806

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr7:131123023-131123049 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
Alleles: del(A)₁₅ / del(A)₁₄ / del(A)₁₃ / d…
del(A)₁₅ / del(A)₁₄ / del(A)₁₃ / del(A)₁₂ / del(A)₁₁ / del(A)₁₀ / del(A)₉ / del(A)₈ / del(A)₇ / del(A)₆ / del(A)₅ / del(A)₄ / delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)₄ / dup(A)₅ / dup(A)₆ / dup(A)₇ / dup(A)₈ / dup(A)₉ / dup(A)₁₀ / dup(A)₁₃ / dup(A)₁₄
Variation Type: Indel Insertion and Deletion
Frequency: del(A)₁₃=0.4800 (2404/5008, 1000G)
del(A)₁₅=0.00 (0/76, ALFA)
del(A)₁₄=0.00 (0/76, ALFA) (+ 23 more)
del(A)₁₃=0.00 (0/76, ALFA)
del(A)₁₂=0.00 (0/76, ALFA)
del(A)₁₁=0.00 (0/76, ALFA)
del(A)₁₀=0.00 (0/76, ALFA)
del(A)₉=0.00 (0/76, ALFA)
del(A)₈=0.00 (0/76, ALFA)
del(A)₇=0.00 (0/76, ALFA)
del(A)₆=0.00 (0/76, ALFA)
del(A)₅=0.00 (0/76, ALFA)
del(A)₄=0.00 (0/76, ALFA)
delAAA=0.00 (0/76, ALFA)
delAA=0.00 (0/76, ALFA)
delA=0.00 (0/76, ALFA)
dupA=0.00 (0/76, ALFA)
dupAA=0.00 (0/76, ALFA)
dupAAA=0.00 (0/76, ALFA)
dup(A)₄=0.00 (0/76, ALFA)
dup(A)₅=0.00 (0/76, ALFA)
dup(A)₆=0.00 (0/76, ALFA)
dup(A)₇=0.00 (0/76, ALFA)
dup(A)₈=0.00 (0/76, ALFA)
dup(A)₉=0.00 (0/76, ALFA)
(A)₂₇=0.10 (4/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: MKLN1 : Intron Variant
Publications: 0 citations
Genomic View: See rs on genome

ALFA Allele Frequency
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.

Release Version: 20231103111315

Population	Group	Sample Size	Ref Allele	Alt Allele	Ref HMOZ	Alt HMOZ	HTRZ	HWEP
Total	Global	76	AAAAAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
European	Sub	16	AAAAAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
African	Sub	56	AAAAAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
African Others	Sub	4	AAAAAAAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
African American	Sub	52	AAAAAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Asian	Sub	0	AAAAAAAAAAAAAAAAAAAAAAAAAAA=0	AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
East Asian	Sub	0	AAAAAAAAAAAAAAAAAAAAAAAAAAA=0	AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Other Asian	Sub	0	AAAAAAAAAAAAAAAAAAAAAAAAAAA=0	AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Latin American 1	Sub	2	AAAAAAAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Latin American 2	Sub	2	AAAAAAAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
South Asian	Sub	0	AAAAAAAAAAAAAAAAAAAAAAAAAAA=0	AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Other	Sub	0	AAAAAAAAAAAAAAAAAAAAAAAAAAA=0	AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
1000Genomes	Global	Study-wide	5008	(A)₂₇=0.5200	del(A)₁₃=0.4800
1000Genomes	African	Sub	1322	(A)₂₇=0.5537	del(A)₁₃=0.4463
1000Genomes	East Asian	Sub	1008	(A)₂₇=0.4653	del(A)₁₃=0.5347
1000Genomes	Europe	Sub	1006	(A)₂₇=0.6342	del(A)₁₃=0.3658
1000Genomes	South Asian	Sub	978	(A)₂₇=0.478	del(A)₁₃=0.522
1000Genomes	American	Sub	694	(A)₂₇=0.429	del(A)₁₃=0.571
Allele Frequency Aggregator	Total	Global	76	(A)₂₇=1.00	del(A)₁₅=0.00, del(A)₁₄=0.00, del(A)₁₃=0.00, del(A)₁₂=0.00, del(A)₁₁=0.00, del(A)₁₀=0.00, del(A)₉=0.00, del(A)₈=0.00, del(A)₇=0.00, del(A)₆=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00, dup(A)₅=0.00, dup(A)₆=0.00, dup(A)₇=0.00, dup(A)₈=0.00, dup(A)₉=0.00
Allele Frequency Aggregator	African	Sub	56	(A)₂₇=1.00	del(A)₁₅=0.00, del(A)₁₄=0.00, del(A)₁₃=0.00, del(A)₁₂=0.00, del(A)₁₁=0.00, del(A)₁₀=0.00, del(A)₉=0.00, del(A)₈=0.00, del(A)₇=0.00, del(A)₆=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00, dup(A)₅=0.00, dup(A)₆=0.00, dup(A)₇=0.00, dup(A)₈=0.00, dup(A)₉=0.00
Allele Frequency Aggregator	European	Sub	16	(A)₂₇=1.00	del(A)₁₅=0.00, del(A)₁₄=0.00, del(A)₁₃=0.00, del(A)₁₂=0.00, del(A)₁₁=0.00, del(A)₁₀=0.00, del(A)₉=0.00, del(A)₈=0.00, del(A)₇=0.00, del(A)₆=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00, dup(A)₅=0.00, dup(A)₆=0.00, dup(A)₇=0.00, dup(A)₈=0.00, dup(A)₉=0.00
Allele Frequency Aggregator	Latin American 1	Sub	2	(A)₂₇=1.0	del(A)₁₅=0.0, del(A)₁₄=0.0, del(A)₁₃=0.0, del(A)₁₂=0.0, del(A)₁₁=0.0, del(A)₁₀=0.0, del(A)₉=0.0, del(A)₈=0.0, del(A)₇=0.0, del(A)₆=0.0, del(A)₅=0.0, del(A)₄=0.0, delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0, dupAAA=0.0, dup(A)₄=0.0, dup(A)₅=0.0, dup(A)₆=0.0, dup(A)₇=0.0, dup(A)₈=0.0, dup(A)₉=0.0
Allele Frequency Aggregator	Latin American 2	Sub	2	(A)₂₇=1.0	del(A)₁₅=0.0, del(A)₁₄=0.0, del(A)₁₃=0.0, del(A)₁₂=0.0, del(A)₁₁=0.0, del(A)₁₀=0.0, del(A)₉=0.0, del(A)₈=0.0, del(A)₇=0.0, del(A)₆=0.0, del(A)₅=0.0, del(A)₄=0.0, delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0, dupAAA=0.0, dup(A)₄=0.0, dup(A)₅=0.0, dup(A)₆=0.0, dup(A)₇=0.0, dup(A)₈=0.0, dup(A)₉=0.0
Allele Frequency Aggregator	South Asian	Sub	0	(A)₂₇=0	del(A)₁₅=0, del(A)₁₄=0, del(A)₁₃=0, del(A)₁₂=0, del(A)₁₁=0, del(A)₁₀=0, del(A)₉=0, del(A)₈=0, del(A)₇=0, del(A)₆=0, del(A)₅=0, del(A)₄=0, delAAA=0, delAA=0, delA=0, dupA=0, dupAA=0, dupAAA=0, dup(A)₄=0, dup(A)₅=0, dup(A)₆=0, dup(A)₇=0, dup(A)₈=0, dup(A)₉=0
Allele Frequency Aggregator	Other	Sub	0	(A)₂₇=0	del(A)₁₅=0, del(A)₁₄=0, del(A)₁₃=0, del(A)₁₂=0, del(A)₁₁=0, del(A)₁₀=0, del(A)₉=0, del(A)₈=0, del(A)₇=0, del(A)₆=0, del(A)₅=0, del(A)₄=0, delAAA=0, delAA=0, delA=0, dupA=0, dupAA=0, dupAAA=0, dup(A)₄=0, dup(A)₅=0, dup(A)₆=0, dup(A)₇=0, dup(A)₈=0, dup(A)₉=0
Allele Frequency Aggregator	Asian	Sub	0	(A)₂₇=0	del(A)₁₅=0, del(A)₁₄=0, del(A)₁₃=0, del(A)₁₂=0, del(A)₁₁=0, del(A)₁₀=0, del(A)₉=0, del(A)₈=0, del(A)₇=0, del(A)₆=0, del(A)₅=0, del(A)₄=0, delAAA=0, delAA=0, delA=0, dupA=0, dupAA=0, dupAAA=0, dup(A)₄=0, dup(A)₅=0, dup(A)₆=0, dup(A)₇=0, dup(A)₈=0, dup(A)₉=0
The Danish reference pan genome	Danish	Study-wide	40	- No frequency provided	dup(A)₄=0.90

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 7	NC_000007.14:g.131123035_131123049del
GRCh38.p14 chr 7	NC_000007.14:g.131123036_131123049del
GRCh38.p14 chr 7	NC_000007.14:g.131123037_131123049del
GRCh38.p14 chr 7	NC_000007.14:g.131123038_131123049del
GRCh38.p14 chr 7	NC_000007.14:g.131123039_131123049del
GRCh38.p14 chr 7	NC_000007.14:g.131123040_131123049del
GRCh38.p14 chr 7	NC_000007.14:g.131123041_131123049del
GRCh38.p14 chr 7	NC_000007.14:g.131123042_131123049del
GRCh38.p14 chr 7	NC_000007.14:g.131123043_131123049del
GRCh38.p14 chr 7	NC_000007.14:g.131123044_131123049del
GRCh38.p14 chr 7	NC_000007.14:g.131123045_131123049del
GRCh38.p14 chr 7	NC_000007.14:g.131123046_131123049del
GRCh38.p14 chr 7	NC_000007.14:g.131123047_131123049del
GRCh38.p14 chr 7	NC_000007.14:g.131123048_131123049del
GRCh38.p14 chr 7	NC_000007.14:g.131123049del
GRCh38.p14 chr 7	NC_000007.14:g.131123049dup
GRCh38.p14 chr 7	NC_000007.14:g.131123048_131123049dup
GRCh38.p14 chr 7	NC_000007.14:g.131123047_131123049dup
GRCh38.p14 chr 7	NC_000007.14:g.131123046_131123049dup
GRCh38.p14 chr 7	NC_000007.14:g.131123045_131123049dup
GRCh38.p14 chr 7	NC_000007.14:g.131123044_131123049dup
GRCh38.p14 chr 7	NC_000007.14:g.131123043_131123049dup
GRCh38.p14 chr 7	NC_000007.14:g.131123042_131123049dup
GRCh38.p14 chr 7	NC_000007.14:g.131123041_131123049dup
GRCh38.p14 chr 7	NC_000007.14:g.131123040_131123049dup
GRCh38.p14 chr 7	NC_000007.14:g.131123037_131123049dup
GRCh38.p14 chr 7	NC_000007.14:g.131123036_131123049dup
GRCh37.p13 chr 7	NC_000007.13:g.130807794_130807808del
GRCh37.p13 chr 7	NC_000007.13:g.130807795_130807808del
GRCh37.p13 chr 7	NC_000007.13:g.130807796_130807808del
GRCh37.p13 chr 7	NC_000007.13:g.130807797_130807808del
GRCh37.p13 chr 7	NC_000007.13:g.130807798_130807808del
GRCh37.p13 chr 7	NC_000007.13:g.130807799_130807808del
GRCh37.p13 chr 7	NC_000007.13:g.130807800_130807808del
GRCh37.p13 chr 7	NC_000007.13:g.130807801_130807808del
GRCh37.p13 chr 7	NC_000007.13:g.130807802_130807808del
GRCh37.p13 chr 7	NC_000007.13:g.130807803_130807808del
GRCh37.p13 chr 7	NC_000007.13:g.130807804_130807808del
GRCh37.p13 chr 7	NC_000007.13:g.130807805_130807808del
GRCh37.p13 chr 7	NC_000007.13:g.130807806_130807808del
GRCh37.p13 chr 7	NC_000007.13:g.130807807_130807808del
GRCh37.p13 chr 7	NC_000007.13:g.130807808del
GRCh37.p13 chr 7	NC_000007.13:g.130807808dup
GRCh37.p13 chr 7	NC_000007.13:g.130807807_130807808dup
GRCh37.p13 chr 7	NC_000007.13:g.130807806_130807808dup
GRCh37.p13 chr 7	NC_000007.13:g.130807805_130807808dup
GRCh37.p13 chr 7	NC_000007.13:g.130807804_130807808dup
GRCh37.p13 chr 7	NC_000007.13:g.130807803_130807808dup
GRCh37.p13 chr 7	NC_000007.13:g.130807802_130807808dup
GRCh37.p13 chr 7	NC_000007.13:g.130807801_130807808dup
GRCh37.p13 chr 7	NC_000007.13:g.130807800_130807808dup
GRCh37.p13 chr 7	NC_000007.13:g.130807799_130807808dup
GRCh37.p13 chr 7	NC_000007.13:g.130807796_130807808dup
GRCh37.p13 chr 7	NC_000007.13:g.130807795_130807808dup

Gene: MKLN1, muskelin 1 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
MKLN1 transcript variant 1	NM_001145354.2:c.-94+1282… NM_001145354.2:c.-94+12828_-94+12842del	N/A	Intron Variant
MKLN1 transcript variant 3	NM_001321316.2:c.	N/A	Genic Upstream Transcript Variant
MKLN1 transcript variant 2	NM_013255.5:c.	N/A	Genic Upstream Transcript Variant
MKLN1 transcript variant X2	XM_047420401.1:c.-94+1282… XM_047420401.1:c.-94+12828_-94+12842del	N/A	Intron Variant
MKLN1 transcript variant X1	XM_006715993.4:c.	N/A	Genic Upstream Transcript Variant
MKLN1 transcript variant X3	XM_011516224.4:c.	N/A	Genic Upstream Transcript Variant
MKLN1 transcript variant X4	XM_047420402.1:c.	N/A	Genic Upstream Transcript Variant

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Not Reported in ClinVar

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement	(A)₂₇=	del(A)₁₅	del(A)₁₄	del(A)₁₃	del(A)₁₂	del(A)₁₁	del(A)₁₀	del(A)₉	del(A)₈	del(A)₇	del(A)₆	del(A)₅	del(A)₄	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄	dup(A)₅	dup(A)₆	dup(A)₇	dup(A)₈	dup(A)₉	dup(A)₁₀	dup(A)₁₃	dup(A)₁₄
GRCh38.p14 chr 7	NC_000007.14:g.131123023_131123049=	NC_000007.14:g.131123035_131123049del	NC_000007.14:g.131123036_131123049del	NC_000007.14:g.131123037_131123049del	NC_000007.14:g.131123038_131123049del	NC_000007.14:g.131123039_131123049del	NC_000007.14:g.131123040_131123049del	NC_000007.14:g.131123041_131123049del	NC_000007.14:g.131123042_131123049del	NC_000007.14:g.131123043_131123049del	NC_000007.14:g.131123044_131123049del	NC_000007.14:g.131123045_131123049del	NC_000007.14:g.131123046_131123049del	NC_000007.14:g.131123047_131123049del	NC_000007.14:g.131123048_131123049del	NC_000007.14:g.131123049del	NC_000007.14:g.131123049dup	NC_000007.14:g.131123048_131123049dup	NC_000007.14:g.131123047_131123049dup	NC_000007.14:g.131123046_131123049dup	NC_000007.14:g.131123045_131123049dup	NC_000007.14:g.131123044_131123049dup	NC_000007.14:g.131123043_131123049dup	NC_000007.14:g.131123042_131123049dup	NC_000007.14:g.131123041_131123049dup	NC_000007.14:g.131123040_131123049dup	NC_000007.14:g.131123037_131123049dup	NC_000007.14:g.131123036_131123049dup
GRCh37.p13 chr 7	NC_000007.13:g.130807782_130807808=	NC_000007.13:g.130807794_130807808del	NC_000007.13:g.130807795_130807808del	NC_000007.13:g.130807796_130807808del	NC_000007.13:g.130807797_130807808del	NC_000007.13:g.130807798_130807808del	NC_000007.13:g.130807799_130807808del	NC_000007.13:g.130807800_130807808del	NC_000007.13:g.130807801_130807808del	NC_000007.13:g.130807802_130807808del	NC_000007.13:g.130807803_130807808del	NC_000007.13:g.130807804_130807808del	NC_000007.13:g.130807805_130807808del	NC_000007.13:g.130807806_130807808del	NC_000007.13:g.130807807_130807808del	NC_000007.13:g.130807808del	NC_000007.13:g.130807808dup	NC_000007.13:g.130807807_130807808dup	NC_000007.13:g.130807806_130807808dup	NC_000007.13:g.130807805_130807808dup	NC_000007.13:g.130807804_130807808dup	NC_000007.13:g.130807803_130807808dup	NC_000007.13:g.130807802_130807808dup	NC_000007.13:g.130807801_130807808dup	NC_000007.13:g.130807800_130807808dup	NC_000007.13:g.130807799_130807808dup	NC_000007.13:g.130807796_130807808dup	NC_000007.13:g.130807795_130807808dup
MKLN1 transcript variant 1	NM_001145354.1:c.-94+12816=	NM_001145354.1:c.-94+12828_-94+12842del	NM_001145354.1:c.-94+12829_-94+12842del	NM_001145354.1:c.-94+12830_-94+12842del	NM_001145354.1:c.-94+12831_-94+12842del	NM_001145354.1:c.-94+12832_-94+12842del	NM_001145354.1:c.-94+12833_-94+12842del	NM_001145354.1:c.-94+12834_-94+12842del	NM_001145354.1:c.-94+12835_-94+12842del	NM_001145354.1:c.-94+12836_-94+12842del	NM_001145354.1:c.-94+12837_-94+12842del	NM_001145354.1:c.-94+12838_-94+12842del	NM_001145354.1:c.-94+12839_-94+12842del	NM_001145354.1:c.-94+12840_-94+12842del	NM_001145354.1:c.-94+12841_-94+12842del	NM_001145354.1:c.-94+12842del	NM_001145354.1:c.-94+12842dup	NM_001145354.1:c.-94+12841_-94+12842dup	NM_001145354.1:c.-94+12840_-94+12842dup	NM_001145354.1:c.-94+12839_-94+12842dup	NM_001145354.1:c.-94+12838_-94+12842dup	NM_001145354.1:c.-94+12837_-94+12842dup	NM_001145354.1:c.-94+12836_-94+12842dup	NM_001145354.1:c.-94+12835_-94+12842dup	NM_001145354.1:c.-94+12834_-94+12842dup	NM_001145354.1:c.-94+12833_-94+12842dup	NM_001145354.1:c.-94+12830_-94+12842dup	NM_001145354.1:c.-94+12829_-94+12842dup
MKLN1 transcript variant 1	NM_001145354.2:c.-94+12816=	NM_001145354.2:c.-94+12828_-94+12842del	NM_001145354.2:c.-94+12829_-94+12842del	NM_001145354.2:c.-94+12830_-94+12842del	NM_001145354.2:c.-94+12831_-94+12842del	NM_001145354.2:c.-94+12832_-94+12842del	NM_001145354.2:c.-94+12833_-94+12842del	NM_001145354.2:c.-94+12834_-94+12842del	NM_001145354.2:c.-94+12835_-94+12842del	NM_001145354.2:c.-94+12836_-94+12842del	NM_001145354.2:c.-94+12837_-94+12842del	NM_001145354.2:c.-94+12838_-94+12842del	NM_001145354.2:c.-94+12839_-94+12842del	NM_001145354.2:c.-94+12840_-94+12842del	NM_001145354.2:c.-94+12841_-94+12842del	NM_001145354.2:c.-94+12842del	NM_001145354.2:c.-94+12842dup	NM_001145354.2:c.-94+12841_-94+12842dup	NM_001145354.2:c.-94+12840_-94+12842dup	NM_001145354.2:c.-94+12839_-94+12842dup	NM_001145354.2:c.-94+12838_-94+12842dup	NM_001145354.2:c.-94+12837_-94+12842dup	NM_001145354.2:c.-94+12836_-94+12842dup	NM_001145354.2:c.-94+12835_-94+12842dup	NM_001145354.2:c.-94+12834_-94+12842dup	NM_001145354.2:c.-94+12833_-94+12842dup	NM_001145354.2:c.-94+12830_-94+12842dup	NM_001145354.2:c.-94+12829_-94+12842dup
MKLN1 transcript variant X2	XM_047420401.1:c.-94+12816=	XM_047420401.1:c.-94+12828_-94+12842del	XM_047420401.1:c.-94+12829_-94+12842del	XM_047420401.1:c.-94+12830_-94+12842del	XM_047420401.1:c.-94+12831_-94+12842del	XM_047420401.1:c.-94+12832_-94+12842del	XM_047420401.1:c.-94+12833_-94+12842del	XM_047420401.1:c.-94+12834_-94+12842del	XM_047420401.1:c.-94+12835_-94+12842del	XM_047420401.1:c.-94+12836_-94+12842del	XM_047420401.1:c.-94+12837_-94+12842del	XM_047420401.1:c.-94+12838_-94+12842del	XM_047420401.1:c.-94+12839_-94+12842del	XM_047420401.1:c.-94+12840_-94+12842del	XM_047420401.1:c.-94+12841_-94+12842del	XM_047420401.1:c.-94+12842del	XM_047420401.1:c.-94+12842dup	XM_047420401.1:c.-94+12841_-94+12842dup	XM_047420401.1:c.-94+12840_-94+12842dup	XM_047420401.1:c.-94+12839_-94+12842dup	XM_047420401.1:c.-94+12838_-94+12842dup	XM_047420401.1:c.-94+12837_-94+12842dup	XM_047420401.1:c.-94+12836_-94+12842dup	XM_047420401.1:c.-94+12835_-94+12842dup	XM_047420401.1:c.-94+12834_-94+12842dup	XM_047420401.1:c.-94+12833_-94+12842dup	XM_047420401.1:c.-94+12830_-94+12842dup	XM_047420401.1:c.-94+12829_-94+12842dup

Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.

62 SubSNP, 42 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss80878470	Dec 15, 2007 (129)
2	HGSV	ss80885477	Dec 15, 2007 (129)
3	HUMANGENOME_JCVI	ss95475381	Feb 06, 2009 (130)
4	PJP	ss295356602	Oct 12, 2018 (152)
5	1000GENOMES	ss1367738282	Aug 21, 2014 (142)
6	EVA_GENOME_DK	ss1577090929	Apr 01, 2015 (144)
7	SWEGEN	ss3002055079	Nov 08, 2017 (151)
8	MCHAISSO	ss3065159098	Nov 08, 2017 (151)
9	URBANLAB	ss3648755184	Oct 12, 2018 (152)
10	EVA_DECODE	ss3720717347	Jul 13, 2019 (153)
11	EVA_DECODE	ss3720717348	Jul 13, 2019 (153)
12	EVA_DECODE	ss3720717349	Jul 13, 2019 (153)
13	EVA_DECODE	ss3720717350	Jul 13, 2019 (153)
14	EVA_DECODE	ss3720717351	Jul 13, 2019 (153)
15	PACBIO	ss3791239682	Jul 13, 2019 (153)
16	KHV_HUMAN_GENOMES	ss3810344697	Jul 13, 2019 (153)
17	EVA	ss3830826153	Apr 26, 2020 (154)
18	GNOMAD	ss4173337189	Apr 26, 2021 (155)
19	GNOMAD	ss4173337190	Apr 26, 2021 (155)
20	GNOMAD	ss4173337191	Apr 26, 2021 (155)
21	GNOMAD	ss4173337192	Apr 26, 2021 (155)
22	GNOMAD	ss4173337193	Apr 26, 2021 (155)
23	GNOMAD	ss4173337194	Apr 26, 2021 (155)
24	GNOMAD	ss4173337195	Apr 26, 2021 (155)
25	GNOMAD	ss4173337196	Apr 26, 2021 (155)
26	GNOMAD	ss4173337197	Apr 26, 2021 (155)
27	GNOMAD	ss4173337198	Apr 26, 2021 (155)
28	GNOMAD	ss4173337199	Apr 26, 2021 (155)
29	GNOMAD	ss4173337200	Apr 26, 2021 (155)
30	GNOMAD	ss4173337201	Apr 26, 2021 (155)
31	GNOMAD	ss4173337202	Apr 26, 2021 (155)
32	GNOMAD	ss4173337203	Apr 26, 2021 (155)
33	GNOMAD	ss4173337204	Apr 26, 2021 (155)
34	GNOMAD	ss4173337205	Apr 26, 2021 (155)
35	GNOMAD	ss4173337206	Apr 26, 2021 (155)
36	GNOMAD	ss4173337207	Apr 26, 2021 (155)
37	GNOMAD	ss4173337208	Apr 26, 2021 (155)
38	GNOMAD	ss4173337209	Apr 26, 2021 (155)
39	GNOMAD	ss4173337210	Apr 26, 2021 (155)
40	GNOMAD	ss4173337211	Apr 26, 2021 (155)
41	GNOMAD	ss4173337212	Apr 26, 2021 (155)
42	GNOMAD	ss4173337213	Apr 26, 2021 (155)
43	GNOMAD	ss4173337214	Apr 26, 2021 (155)
44	GNOMAD	ss4173337215	Apr 26, 2021 (155)
45	TOMMO_GENOMICS	ss5185643199	Apr 26, 2021 (155)
46	TOMMO_GENOMICS	ss5185643200	Apr 26, 2021 (155)
47	TOMMO_GENOMICS	ss5185643201	Apr 26, 2021 (155)
48	TOMMO_GENOMICS	ss5185643202	Apr 26, 2021 (155)
49	TOMMO_GENOMICS	ss5185643203	Apr 26, 2021 (155)
50	TOMMO_GENOMICS	ss5185643204	Apr 26, 2021 (155)
51	1000G_HIGH_COVERAGE	ss5274784600	Oct 13, 2022 (156)
52	1000G_HIGH_COVERAGE	ss5274784601	Oct 13, 2022 (156)
53	HUGCELL_USP	ss5471665561	Oct 13, 2022 (156)
54	HUGCELL_USP	ss5471665562	Oct 13, 2022 (156)
55	HUGCELL_USP	ss5471665563	Oct 13, 2022 (156)
56	HUGCELL_USP	ss5471665564	Oct 13, 2022 (156)
57	TOMMO_GENOMICS	ss5726655774	Oct 13, 2022 (156)
58	TOMMO_GENOMICS	ss5726655775	Oct 13, 2022 (156)
59	TOMMO_GENOMICS	ss5726655776	Oct 13, 2022 (156)
60	TOMMO_GENOMICS	ss5726655777	Oct 13, 2022 (156)
61	TOMMO_GENOMICS	ss5726655778	Oct 13, 2022 (156)
62	TOMMO_GENOMICS	ss5726655779	Oct 13, 2022 (156)
63	1000Genomes	NC_000007.13 - 130807782	Oct 12, 2018 (152)
64	The Danish reference pan genome	NC_000007.13 - 130807782	Apr 26, 2020 (154)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 277044786 (NC_000007.14:131123022::A 24583/56628) Row 277044787 (NC_000007.14:131123022::AA 7595/57032) Row 277044788 (NC_000007.14:131123022::AAA 3285/57158)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 277044786 (NC_000007.14:131123022::A 24583/56628) Row 277044787 (NC_000007.14:131123022::AA 7595/57032) Row 277044788 (NC_000007.14:131123022::AAA 3285/57158)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 277044786 (NC_000007.14:131123022::A 24583/56628) Row 277044787 (NC_000007.14:131123022::AA 7595/57032) Row 277044788 (NC_000007.14:131123022::AAA 3285/57158)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 277044786 (NC_000007.14:131123022::A 24583/56628) Row 277044787 (NC_000007.14:131123022::AA 7595/57032) Row 277044788 (NC_000007.14:131123022::AAA 3285/57158)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 277044786 (NC_000007.14:131123022::A 24583/56628) Row 277044787 (NC_000007.14:131123022::AA 7595/57032) Row 277044788 (NC_000007.14:131123022::AAA 3285/57158)...	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 277044786 (NC_000007.14:131123022::A 24583/56628) Row 277044787 (NC_000007.14:131123022::AA 7595/57032) Row 277044788 (NC_000007.14:131123022::AAA 3285/57158)...	-	Apr 26, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 277044786 (NC_000007.14:131123022::A 24583/56628) Row 277044787 (NC_000007.14:131123022::AA 7595/57032) Row 277044788 (NC_000007.14:131123022::AAA 3285/57158)...	-	Apr 26, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 277044786 (NC_000007.14:131123022::A 24583/56628) Row 277044787 (NC_000007.14:131123022::AA 7595/57032) Row 277044788 (NC_000007.14:131123022::AAA 3285/57158)...	-	Apr 26, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 277044786 (NC_000007.14:131123022::A 24583/56628) Row 277044787 (NC_000007.14:131123022::AA 7595/57032) Row 277044788 (NC_000007.14:131123022::AAA 3285/57158)...	-	Apr 26, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 277044786 (NC_000007.14:131123022::A 24583/56628) Row 277044787 (NC_000007.14:131123022::AA 7595/57032) Row 277044788 (NC_000007.14:131123022::AAA 3285/57158)...	-	Apr 26, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 277044786 (NC_000007.14:131123022::A 24583/56628) Row 277044787 (NC_000007.14:131123022::AA 7595/57032) Row 277044788 (NC_000007.14:131123022::AAA 3285/57158)...	-	Apr 26, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 277044786 (NC_000007.14:131123022::A 24583/56628) Row 277044787 (NC_000007.14:131123022::AA 7595/57032) Row 277044788 (NC_000007.14:131123022::AAA 3285/57158)...	-	Apr 26, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 277044786 (NC_000007.14:131123022::A 24583/56628) Row 277044787 (NC_000007.14:131123022::AA 7595/57032) Row 277044788 (NC_000007.14:131123022::AAA 3285/57158)...	-	Apr 26, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 277044786 (NC_000007.14:131123022::A 24583/56628) Row 277044787 (NC_000007.14:131123022::AA 7595/57032) Row 277044788 (NC_000007.14:131123022::AAA 3285/57158)...	-	Apr 26, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 277044786 (NC_000007.14:131123022::A 24583/56628) Row 277044787 (NC_000007.14:131123022::AA 7595/57032) Row 277044788 (NC_000007.14:131123022::AAA 3285/57158)...	-	Apr 26, 2021 (155)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 277044786 (NC_000007.14:131123022::A 24583/56628) Row 277044787 (NC_000007.14:131123022::AA 7595/57032) Row 277044788 (NC_000007.14:131123022::AAA 3285/57158)...	-	Apr 26, 2021 (155)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 277044786 (NC_000007.14:131123022::A 24583/56628) Row 277044787 (NC_000007.14:131123022::AA 7595/57032) Row 277044788 (NC_000007.14:131123022::AAA 3285/57158)...	-	Apr 26, 2021 (155)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 277044786 (NC_000007.14:131123022::A 24583/56628) Row 277044787 (NC_000007.14:131123022::AA 7595/57032) Row 277044788 (NC_000007.14:131123022::AAA 3285/57158)...	-	Apr 26, 2021 (155)
83	gnomAD - Genomes Submission ignored due to conflicting rows: Row 277044786 (NC_000007.14:131123022::A 24583/56628) Row 277044787 (NC_000007.14:131123022::AA 7595/57032) Row 277044788 (NC_000007.14:131123022::AAA 3285/57158)...	-	Apr 26, 2021 (155)
84	gnomAD - Genomes Submission ignored due to conflicting rows: Row 277044786 (NC_000007.14:131123022::A 24583/56628) Row 277044787 (NC_000007.14:131123022::AA 7595/57032) Row 277044788 (NC_000007.14:131123022::AAA 3285/57158)...	-	Apr 26, 2021 (155)
85	gnomAD - Genomes Submission ignored due to conflicting rows: Row 277044786 (NC_000007.14:131123022::A 24583/56628) Row 277044787 (NC_000007.14:131123022::AA 7595/57032) Row 277044788 (NC_000007.14:131123022::AAA 3285/57158)...	-	Apr 26, 2021 (155)
86	gnomAD - Genomes Submission ignored due to conflicting rows: Row 277044786 (NC_000007.14:131123022::A 24583/56628) Row 277044787 (NC_000007.14:131123022::AA 7595/57032) Row 277044788 (NC_000007.14:131123022::AAA 3285/57158)...	-	Apr 26, 2021 (155)
87	gnomAD - Genomes Submission ignored due to conflicting rows: Row 277044786 (NC_000007.14:131123022::A 24583/56628) Row 277044787 (NC_000007.14:131123022::AA 7595/57032) Row 277044788 (NC_000007.14:131123022::AAA 3285/57158)...	-	Apr 26, 2021 (155)
88	gnomAD - Genomes Submission ignored due to conflicting rows: Row 277044786 (NC_000007.14:131123022::A 24583/56628) Row 277044787 (NC_000007.14:131123022::AA 7595/57032) Row 277044788 (NC_000007.14:131123022::AAA 3285/57158)...	-	Apr 26, 2021 (155)
89	gnomAD - Genomes Submission ignored due to conflicting rows: Row 277044786 (NC_000007.14:131123022::A 24583/56628) Row 277044787 (NC_000007.14:131123022::AA 7595/57032) Row 277044788 (NC_000007.14:131123022::AAA 3285/57158)...	-	Apr 26, 2021 (155)
90	gnomAD - Genomes Submission ignored due to conflicting rows: Row 277044786 (NC_000007.14:131123022::A 24583/56628) Row 277044787 (NC_000007.14:131123022::AA 7595/57032) Row 277044788 (NC_000007.14:131123022::AAA 3285/57158)...	-	Apr 26, 2021 (155)
91	gnomAD - Genomes Submission ignored due to conflicting rows: Row 277044786 (NC_000007.14:131123022::A 24583/56628) Row 277044787 (NC_000007.14:131123022::AA 7595/57032) Row 277044788 (NC_000007.14:131123022::AAA 3285/57158)...	-	Apr 26, 2021 (155)
92	8.3KJPN Submission ignored due to conflicting rows: Row 43612506 (NC_000007.13:130807781:AAAAAAAAAAAAA: 614/11444) Row 43612507 (NC_000007.13:130807781::A 1076/11444) Row 43612508 (NC_000007.13:130807781::AAAA 2157/11444)...	-	Apr 26, 2021 (155)
93	8.3KJPN Submission ignored due to conflicting rows: Row 43612506 (NC_000007.13:130807781:AAAAAAAAAAAAA: 614/11444) Row 43612507 (NC_000007.13:130807781::A 1076/11444) Row 43612508 (NC_000007.13:130807781::AAAA 2157/11444)...	-	Apr 26, 2021 (155)
94	8.3KJPN Submission ignored due to conflicting rows: Row 43612506 (NC_000007.13:130807781:AAAAAAAAAAAAA: 614/11444) Row 43612507 (NC_000007.13:130807781::A 1076/11444) Row 43612508 (NC_000007.13:130807781::AAAA 2157/11444)...	-	Apr 26, 2021 (155)
95	8.3KJPN Submission ignored due to conflicting rows: Row 43612506 (NC_000007.13:130807781:AAAAAAAAAAAAA: 614/11444) Row 43612507 (NC_000007.13:130807781::A 1076/11444) Row 43612508 (NC_000007.13:130807781::AAAA 2157/11444)...	-	Apr 26, 2021 (155)
96	8.3KJPN Submission ignored due to conflicting rows: Row 43612506 (NC_000007.13:130807781:AAAAAAAAAAAAA: 614/11444) Row 43612507 (NC_000007.13:130807781::A 1076/11444) Row 43612508 (NC_000007.13:130807781::AAAA 2157/11444)...	-	Apr 26, 2021 (155)
97	8.3KJPN Submission ignored due to conflicting rows: Row 43612506 (NC_000007.13:130807781:AAAAAAAAAAAAA: 614/11444) Row 43612507 (NC_000007.13:130807781::A 1076/11444) Row 43612508 (NC_000007.13:130807781::AAAA 2157/11444)...	-	Apr 26, 2021 (155)
98	14KJPN Submission ignored due to conflicting rows: Row 60492878 (NC_000007.14:131123022:AAAAAAAAAAAAA: 1276/19902) Row 60492879 (NC_000007.14:131123022::AA 2939/19902) Row 60492880 (NC_000007.14:131123022::A 2217/19902)...	-	Oct 13, 2022 (156)
99	14KJPN Submission ignored due to conflicting rows: Row 60492878 (NC_000007.14:131123022:AAAAAAAAAAAAA: 1276/19902) Row 60492879 (NC_000007.14:131123022::AA 2939/19902) Row 60492880 (NC_000007.14:131123022::A 2217/19902)...	-	Oct 13, 2022 (156)
100	14KJPN Submission ignored due to conflicting rows: Row 60492878 (NC_000007.14:131123022:AAAAAAAAAAAAA: 1276/19902) Row 60492879 (NC_000007.14:131123022::AA 2939/19902) Row 60492880 (NC_000007.14:131123022::A 2217/19902)...	-	Oct 13, 2022 (156)
101	14KJPN Submission ignored due to conflicting rows: Row 60492878 (NC_000007.14:131123022:AAAAAAAAAAAAA: 1276/19902) Row 60492879 (NC_000007.14:131123022::AA 2939/19902) Row 60492880 (NC_000007.14:131123022::A 2217/19902)...	-	Oct 13, 2022 (156)
102	14KJPN Submission ignored due to conflicting rows: Row 60492878 (NC_000007.14:131123022:AAAAAAAAAAAAA: 1276/19902) Row 60492879 (NC_000007.14:131123022::AA 2939/19902) Row 60492880 (NC_000007.14:131123022::A 2217/19902)...	-	Oct 13, 2022 (156)
103	14KJPN Submission ignored due to conflicting rows: Row 60492878 (NC_000007.14:131123022:AAAAAAAAAAAAA: 1276/19902) Row 60492879 (NC_000007.14:131123022::AA 2939/19902) Row 60492880 (NC_000007.14:131123022::A 2217/19902)...	-	Oct 13, 2022 (156)
104	ALFA	NC_000007.14 - 131123023	Apr 26, 2021 (155)

History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4173337215	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAA:	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
9042069444	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss4173337214	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAA:	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
9042069444	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
39231806, ss1367738282, ss3002055079, ss5185643199	NC_000007.13:130807781:AAAAAAAAAAA… NC_000007.13:130807781:AAAAAAAAAAAAA:	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3065159098, ss3720717351, ss3810344697, ss4173337213, ss5274784600, ss5471665563, ss5726655774	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAA:	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
9042069444	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss4173337212	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAA:	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
9042069444	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss4173337211	NC_000007.14:131123022:AAAAAAAAAAA:	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
9042069444	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss4173337210	NC_000007.14:131123022:AAAAAAAAAA:	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
9042069444	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss4173337209	NC_000007.14:131123022:AAAAAAAAA:	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
9042069444	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4173337208	NC_000007.14:131123022:AAAAAAAA:	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
9042069444	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss4173337207	NC_000007.14:131123022:AAAAAAA:	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
9042069444	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss4173337206	NC_000007.14:131123022:AAAAAA:	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
9042069444	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss4173337205	NC_000007.14:131123022:AAAAA:	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
9042069444	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss4173337204	NC_000007.14:131123022:AAAA:	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
9042069444	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4173337203	NC_000007.14:131123022:AAA:	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
9042069444	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4173337202	NC_000007.14:131123022:AA:	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
9042069444	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4173337201	NC_000007.14:131123022:A:	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
9042069444	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss295356602	NC_000007.12:130458322::A	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5185643200	NC_000007.13:130807781::A	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3648755184, ss4173337189, ss5471665561, ss5726655776	NC_000007.14:131123022::A	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
9042069444	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3720717350	NC_000007.14:131123035::A	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss95475381	NT_007933.15:68840651::A	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5185643204	NC_000007.13:130807781::AA	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4173337190, ss5471665562, ss5726655775	NC_000007.14:131123022::AA	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
9042069444	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3720717349	NC_000007.14:131123035::AA	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3791239682	NC_000007.13:130807781::AAA	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4173337191, ss5471665564, ss5726655779	NC_000007.14:131123022::AAA	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
9042069444	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3720717348	NC_000007.14:131123035::AAA	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss80878470, ss80885477	NT_007933.15:68840651::AAA	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
1184696, ss1577090929, ss3830826153, ss5185643201	NC_000007.13:130807781::AAAA	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4173337192, ss5726655777	NC_000007.14:131123022::AAAA	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
9042069444	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3720717347	NC_000007.14:131123035::AAAA	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4173337193, ss5274784601	NC_000007.14:131123022::AAAAA	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
9042069444	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5185643203	NC_000007.13:130807781::AAAAAA	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4173337194, ss5726655778	NC_000007.14:131123022::AAAAAA	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
9042069444	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5185643202	NC_000007.13:130807781::AAAAAAA	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4173337195	NC_000007.14:131123022::AAAAAAA	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
9042069444	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4173337196	NC_000007.14:131123022::AAAAAAAA	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
9042069444	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4173337197	NC_000007.14:131123022::AAAAAAAAA	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
9042069444	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4173337198	NC_000007.14:131123022::AAAAAAAAAA	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4173337199	NC_000007.14:131123022::AAAAAAAAAA… NC_000007.14:131123022::AAAAAAAAAAAAA	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4173337200	NC_000007.14:131123022::AAAAAAAAAA… NC_000007.14:131123022::AAAAAAAAAAAAAA	NC_000007.14:131123022:AAAAAAAAAAA… NC_000007.14:131123022:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs59581806

The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.

Genome context:

Select flank length:

Genomic regions, transcripts, and products
Top▲ Help
NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

Choose placement

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs59581806