Name: rs1203391424
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.

rs1203391424

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr4:46076363-46076404 (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(AT)₁₆ / del(AT)₁₅ / del(AT)₁₄ …
del(AT)₁₆ / del(AT)₁₅ / del(AT)₁₄ / del(AT)₁₃ / del(AT)₁₂ / del(AT)₁₁ / del(AT)₁₀ / del(AT)₉ / del(AT)₈ / del(AT)₇ / del(AT)₆ / del(AT)₅ / del(AT)₄ / del(AT)₃ / delATAT / delAT / dupAT / dupATAT / dup(AT)₃ / dup(AT)₄ / dup(AT)₅ / dup(AT)₆
Variation Type: Indel Insertion and Deletion
Frequency: del(AT)₁₆=0.0000 (0/7228, ALFA)
del(AT)₁₅=0.0000 (0/7228, ALFA)
del(AT)₁₄=0.0000 (0/7228, ALFA) (+ 19 more)
del(AT)₁₃=0.0000 (0/7228, ALFA)
del(AT)₁₂=0.0000 (0/7228, ALFA)
del(AT)₁₁=0.0000 (0/7228, ALFA)
del(AT)₁₀=0.0000 (0/7228, ALFA)
del(AT)₉=0.0000 (0/7228, ALFA)
del(AT)₈=0.0000 (0/7228, ALFA)
del(AT)₇=0.0000 (0/7228, ALFA)
del(AT)₆=0.0000 (0/7228, ALFA)
del(AT)₅=0.0000 (0/7228, ALFA)
del(AT)₄=0.0000 (0/7228, ALFA)
del(AT)₃=0.0000 (0/7228, ALFA)
delATAT=0.0000 (0/7228, ALFA)
delAT=0.0000 (0/7228, ALFA)
dupAT=0.0000 (0/7228, ALFA)
dupATAT=0.0000 (0/7228, ALFA)
dup(AT)₃=0.0000 (0/7228, ALFA)
dup(AT)₄=0.0000 (0/7228, ALFA)
dup(AT)₅=0.0000 (0/7228, ALFA)
dup(AT)₆=0.0000 (0/7228, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: GABRG1 : 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	HWEP
Total	Global	7228	ATATATATATATATATATATATATATATATATATATATATAT=1.0000	ATATATATAT=0.0000, ATATATATATAT=0.0000, ATATATATATATAT=0.0000, ATATATATATATATAT=0.0000, ATATATATATATATATAT=0.0000, ATATATATATATATATATAT=0.0000, ATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATATATATATATATATATATATATAT=0.0000	1.0	N/A
European	Sub	4740	ATATATATATATATATATATATATATATATATATATATATAT=1.0000	ATATATATAT=0.0000, ATATATATATAT=0.0000, ATATATATATATAT=0.0000, ATATATATATATATAT=0.0000, ATATATATATATATATAT=0.0000, ATATATATATATATATATAT=0.0000, ATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATATATATATATATATATATATATAT=0.0000	1.0	N/A
African	Sub	1710	ATATATATATATATATATATATATATATATATATATATATAT=1.0000	ATATATATAT=0.0000, ATATATATATAT=0.0000, ATATATATATATAT=0.0000, ATATATATATATATAT=0.0000, ATATATATATATATATAT=0.0000, ATATATATATATATATATAT=0.0000, ATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATATATATATATATATATATATATAT=0.0000	1.0	N/A
African Others	Sub	64	ATATATATATATATATATATATATATATATATATATATATAT=1.00	ATATATATAT=0.00, ATATATATATAT=0.00, ATATATATATATAT=0.00, ATATATATATATATAT=0.00, ATATATATATATATATAT=0.00, ATATATATATATATATATAT=0.00, ATATATATATATATATATATAT=0.00, ATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATATATATATATATATATATAT=0.00	1.0	N/A
African American	Sub	1646	ATATATATATATATATATATATATATATATATATATATATAT=1.0000	ATATATATAT=0.0000, ATATATATATAT=0.0000, ATATATATATATAT=0.0000, ATATATATATATATAT=0.0000, ATATATATATATATATAT=0.0000, ATATATATATATATATATAT=0.0000, ATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATATATATATATATATATATATAT=0.0000, ATATATATATATATATATATATATATATATATATATATATATATATATATATAT=0.0000	1.0	N/A
Asian	Sub	38	ATATATATATATATATATATATATATATATATATATATATAT=1.00	ATATATATAT=0.00, ATATATATATAT=0.00, ATATATATATATAT=0.00, ATATATATATATATAT=0.00, ATATATATATATATATAT=0.00, ATATATATATATATATATAT=0.00, ATATATATATATATATATATAT=0.00, ATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATATATATATATATATATATAT=0.00	1.0	N/A
East Asian	Sub	28	ATATATATATATATATATATATATATATATATATATATATAT=1.00	ATATATATAT=0.00, ATATATATATAT=0.00, ATATATATATATAT=0.00, ATATATATATATATAT=0.00, ATATATATATATATATAT=0.00, ATATATATATATATATATAT=0.00, ATATATATATATATATATATAT=0.00, ATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATATATATATATATATATATAT=0.00	1.0	N/A
Other Asian	Sub	10	ATATATATATATATATATATATATATATATATATATATATAT=1.0	ATATATATAT=0.0, ATATATATATAT=0.0, ATATATATATATAT=0.0, ATATATATATATATAT=0.0, ATATATATATATATATAT=0.0, ATATATATATATATATATAT=0.0, ATATATATATATATATATATAT=0.0, ATATATATATATATATATATATAT=0.0, ATATATATATATATATATATATATAT=0.0, ATATATATATATATATATATATATATAT=0.0, ATATATATATATATATATATATATATATAT=0.0, ATATATATATATATATATATATATATATATAT=0.0, ATATATATATATATATATATATATATATATATAT=0.0, ATATATATATATATATATATATATATATATATATAT=0.0, ATATATATATATATATATATATATATATATATATATAT=0.0, ATATATATATATATATATATATATATATATATATATATAT=0.0, ATATATATATATATATATATATATATATATATATATATATATAT=0.0, ATATATATATATATATATATATATATATATATATATATATATATAT=0.0, ATATATATATATATATATATATATATATATATATATATATATATATAT=0.0, ATATATATATATATATATATATATATATATATATATATATATATATATAT=0.0, ATATATATATATATATATATATATATATATATATATATATATATATATATAT=0.0, ATATATATATATATATATATATATATATATATATATATATATATATATATATAT=0.0	1.0	N/A
Latin American 1	Sub	84	ATATATATATATATATATATATATATATATATATATATATAT=1.00	ATATATATAT=0.00, ATATATATATAT=0.00, ATATATATATATAT=0.00, ATATATATATATATAT=0.00, ATATATATATATATATAT=0.00, ATATATATATATATATATAT=0.00, ATATATATATATATATATATAT=0.00, ATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATATATATATATATATATATAT=0.00	1.0	N/A
Latin American 2	Sub	346	ATATATATATATATATATATATATATATATATATATATATAT=1.000	ATATATATAT=0.000, ATATATATATAT=0.000, ATATATATATATAT=0.000, ATATATATATATATAT=0.000, ATATATATATATATATAT=0.000, ATATATATATATATATATAT=0.000, ATATATATATATATATATATAT=0.000, ATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATATATATATATATATATATATATATAT=0.000	1.0	N/A
South Asian	Sub	32	ATATATATATATATATATATATATATATATATATATATATAT=1.00	ATATATATAT=0.00, ATATATATATAT=0.00, ATATATATATATAT=0.00, ATATATATATATATAT=0.00, ATATATATATATATATAT=0.00, ATATATATATATATATATAT=0.00, ATATATATATATATATATATAT=0.00, ATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATATATATATATATATATAT=0.00, ATATATATATATATATATATATATATATATATATATATATATATATATATATAT=0.00	1.0	N/A
Other	Sub	278	ATATATATATATATATATATATATATATATATATATATATAT=1.000	ATATATATAT=0.000, ATATATATATAT=0.000, ATATATATATATAT=0.000, ATATATATATATATAT=0.000, ATATATATATATATATAT=0.000, ATATATATATATATATATAT=0.000, ATATATATATATATATATATAT=0.000, ATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATATATATATATATATATATATATAT=0.000, ATATATATATATATATATATATATATATATATATATATATATATATATATATAT=0.000	1.0	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").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	7228	(AT)₂₁=1.0000	del(AT)₁₆=0.0000, del(AT)₁₅=0.0000, del(AT)₁₄=0.0000, del(AT)₁₃=0.0000, del(AT)₁₂=0.0000, del(AT)₁₁=0.0000, del(AT)₁₀=0.0000, del(AT)₉=0.0000, del(AT)₈=0.0000, del(AT)₇=0.0000, del(AT)₆=0.0000, del(AT)₅=0.0000, del(AT)₄=0.0000, del(AT)₃=0.0000, delATAT=0.0000, delAT=0.0000, dupAT=0.0000, dupATAT=0.0000, dup(AT)₃=0.0000, dup(AT)₄=0.0000, dup(AT)₅=0.0000, dup(AT)₆=0.0000
Allele Frequency Aggregator	European	Sub	4740	(AT)₂₁=1.0000	del(AT)₁₆=0.0000, del(AT)₁₅=0.0000, del(AT)₁₄=0.0000, del(AT)₁₃=0.0000, del(AT)₁₂=0.0000, del(AT)₁₁=0.0000, del(AT)₁₀=0.0000, del(AT)₉=0.0000, del(AT)₈=0.0000, del(AT)₇=0.0000, del(AT)₆=0.0000, del(AT)₅=0.0000, del(AT)₄=0.0000, del(AT)₃=0.0000, delATAT=0.0000, delAT=0.0000, dupAT=0.0000, dupATAT=0.0000, dup(AT)₃=0.0000, dup(AT)₄=0.0000, dup(AT)₅=0.0000, dup(AT)₆=0.0000
Allele Frequency Aggregator	African	Sub	1710	(AT)₂₁=1.0000	del(AT)₁₆=0.0000, del(AT)₁₅=0.0000, del(AT)₁₄=0.0000, del(AT)₁₃=0.0000, del(AT)₁₂=0.0000, del(AT)₁₁=0.0000, del(AT)₁₀=0.0000, del(AT)₉=0.0000, del(AT)₈=0.0000, del(AT)₇=0.0000, del(AT)₆=0.0000, del(AT)₅=0.0000, del(AT)₄=0.0000, del(AT)₃=0.0000, delATAT=0.0000, delAT=0.0000, dupAT=0.0000, dupATAT=0.0000, dup(AT)₃=0.0000, dup(AT)₄=0.0000, dup(AT)₅=0.0000, dup(AT)₆=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	346	(AT)₂₁=1.000	del(AT)₁₆=0.000, del(AT)₁₅=0.000, del(AT)₁₄=0.000, del(AT)₁₃=0.000, del(AT)₁₂=0.000, del(AT)₁₁=0.000, del(AT)₁₀=0.000, del(AT)₉=0.000, del(AT)₈=0.000, del(AT)₇=0.000, del(AT)₆=0.000, del(AT)₅=0.000, del(AT)₄=0.000, del(AT)₃=0.000, delATAT=0.000, delAT=0.000, dupAT=0.000, dupATAT=0.000, dup(AT)₃=0.000, dup(AT)₄=0.000, dup(AT)₅=0.000, dup(AT)₆=0.000
Allele Frequency Aggregator	Other	Sub	278	(AT)₂₁=1.000	del(AT)₁₆=0.000, del(AT)₁₅=0.000, del(AT)₁₄=0.000, del(AT)₁₃=0.000, del(AT)₁₂=0.000, del(AT)₁₁=0.000, del(AT)₁₀=0.000, del(AT)₉=0.000, del(AT)₈=0.000, del(AT)₇=0.000, del(AT)₆=0.000, del(AT)₅=0.000, del(AT)₄=0.000, del(AT)₃=0.000, delATAT=0.000, delAT=0.000, dupAT=0.000, dupATAT=0.000, dup(AT)₃=0.000, dup(AT)₄=0.000, dup(AT)₅=0.000, dup(AT)₆=0.000
Allele Frequency Aggregator	Latin American 1	Sub	84	(AT)₂₁=1.00	del(AT)₁₆=0.00, del(AT)₁₅=0.00, del(AT)₁₄=0.00, del(AT)₁₃=0.00, del(AT)₁₂=0.00, del(AT)₁₁=0.00, del(AT)₁₀=0.00, del(AT)₉=0.00, del(AT)₈=0.00, del(AT)₇=0.00, del(AT)₆=0.00, del(AT)₅=0.00, del(AT)₄=0.00, del(AT)₃=0.00, delATAT=0.00, delAT=0.00, dupAT=0.00, dupATAT=0.00, dup(AT)₃=0.00, dup(AT)₄=0.00, dup(AT)₅=0.00, dup(AT)₆=0.00
Allele Frequency Aggregator	Asian	Sub	38	(AT)₂₁=1.00	del(AT)₁₆=0.00, del(AT)₁₅=0.00, del(AT)₁₄=0.00, del(AT)₁₃=0.00, del(AT)₁₂=0.00, del(AT)₁₁=0.00, del(AT)₁₀=0.00, del(AT)₉=0.00, del(AT)₈=0.00, del(AT)₇=0.00, del(AT)₆=0.00, del(AT)₅=0.00, del(AT)₄=0.00, del(AT)₃=0.00, delATAT=0.00, delAT=0.00, dupAT=0.00, dupATAT=0.00, dup(AT)₃=0.00, dup(AT)₄=0.00, dup(AT)₅=0.00, dup(AT)₆=0.00
Allele Frequency Aggregator	South Asian	Sub	32	(AT)₂₁=1.00	del(AT)₁₆=0.00, del(AT)₁₅=0.00, del(AT)₁₄=0.00, del(AT)₁₃=0.00, del(AT)₁₂=0.00, del(AT)₁₁=0.00, del(AT)₁₀=0.00, del(AT)₉=0.00, del(AT)₈=0.00, del(AT)₇=0.00, del(AT)₆=0.00, del(AT)₅=0.00, del(AT)₄=0.00, del(AT)₃=0.00, delATAT=0.00, delAT=0.00, dupAT=0.00, dupATAT=0.00, dup(AT)₃=0.00, dup(AT)₄=0.00, dup(AT)₅=0.00, dup(AT)₆=0.00

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 4	NC_000004.12:g.46076363AT[5]
GRCh38.p14 chr 4	NC_000004.12:g.46076363AT[6]
GRCh38.p14 chr 4	NC_000004.12:g.46076363AT[7]
GRCh38.p14 chr 4	NC_000004.12:g.46076363AT[8]
GRCh38.p14 chr 4	NC_000004.12:g.46076363AT[9]
GRCh38.p14 chr 4	NC_000004.12:g.46076363AT[10]
GRCh38.p14 chr 4	NC_000004.12:g.46076363AT[11]
GRCh38.p14 chr 4	NC_000004.12:g.46076363AT[12]
GRCh38.p14 chr 4	NC_000004.12:g.46076363AT[13]
GRCh38.p14 chr 4	NC_000004.12:g.46076363AT[14]
GRCh38.p14 chr 4	NC_000004.12:g.46076363AT[15]
GRCh38.p14 chr 4	NC_000004.12:g.46076363AT[16]
GRCh38.p14 chr 4	NC_000004.12:g.46076363AT[17]
GRCh38.p14 chr 4	NC_000004.12:g.46076363AT[18]
GRCh38.p14 chr 4	NC_000004.12:g.46076363AT[19]
GRCh38.p14 chr 4	NC_000004.12:g.46076363AT[20]
GRCh38.p14 chr 4	NC_000004.12:g.46076363AT[22]
GRCh38.p14 chr 4	NC_000004.12:g.46076363AT[23]
GRCh38.p14 chr 4	NC_000004.12:g.46076363AT[24]
GRCh38.p14 chr 4	NC_000004.12:g.46076363AT[25]
GRCh38.p14 chr 4	NC_000004.12:g.46076363AT[26]
GRCh38.p14 chr 4	NC_000004.12:g.46076363AT[27]
GRCh37.p13 chr 4	NC_000004.11:g.46078380AT[5]
GRCh37.p13 chr 4	NC_000004.11:g.46078380AT[6]
GRCh37.p13 chr 4	NC_000004.11:g.46078380AT[7]
GRCh37.p13 chr 4	NC_000004.11:g.46078380AT[8]
GRCh37.p13 chr 4	NC_000004.11:g.46078380AT[9]
GRCh37.p13 chr 4	NC_000004.11:g.46078380AT[10]
GRCh37.p13 chr 4	NC_000004.11:g.46078380AT[11]
GRCh37.p13 chr 4	NC_000004.11:g.46078380AT[12]
GRCh37.p13 chr 4	NC_000004.11:g.46078380AT[13]
GRCh37.p13 chr 4	NC_000004.11:g.46078380AT[14]
GRCh37.p13 chr 4	NC_000004.11:g.46078380AT[15]
GRCh37.p13 chr 4	NC_000004.11:g.46078380AT[16]
GRCh37.p13 chr 4	NC_000004.11:g.46078380AT[17]
GRCh37.p13 chr 4	NC_000004.11:g.46078380AT[18]
GRCh37.p13 chr 4	NC_000004.11:g.46078380AT[19]
GRCh37.p13 chr 4	NC_000004.11:g.46078380AT[20]
GRCh37.p13 chr 4	NC_000004.11:g.46078380AT[22]
GRCh37.p13 chr 4	NC_000004.11:g.46078380AT[23]
GRCh37.p13 chr 4	NC_000004.11:g.46078380AT[24]
GRCh37.p13 chr 4	NC_000004.11:g.46078380AT[25]
GRCh37.p13 chr 4	NC_000004.11:g.46078380AT[26]
GRCh37.p13 chr 4	NC_000004.11:g.46078380AT[27]
GABRG1 RefSeqGene	NG_046964.1:g.52662AT[5]
GABRG1 RefSeqGene	NG_046964.1:g.52662AT[6]
GABRG1 RefSeqGene	NG_046964.1:g.52662AT[7]
GABRG1 RefSeqGene	NG_046964.1:g.52662AT[8]
GABRG1 RefSeqGene	NG_046964.1:g.52662AT[9]
GABRG1 RefSeqGene	NG_046964.1:g.52662AT[10]
GABRG1 RefSeqGene	NG_046964.1:g.52662AT[11]
GABRG1 RefSeqGene	NG_046964.1:g.52662AT[12]
GABRG1 RefSeqGene	NG_046964.1:g.52662AT[13]
GABRG1 RefSeqGene	NG_046964.1:g.52662AT[14]
GABRG1 RefSeqGene	NG_046964.1:g.52662AT[15]
GABRG1 RefSeqGene	NG_046964.1:g.52662AT[16]
GABRG1 RefSeqGene	NG_046964.1:g.52662AT[17]
GABRG1 RefSeqGene	NG_046964.1:g.52662AT[18]
GABRG1 RefSeqGene	NG_046964.1:g.52662AT[19]
GABRG1 RefSeqGene	NG_046964.1:g.52662AT[20]
GABRG1 RefSeqGene	NG_046964.1:g.52662AT[22]
GABRG1 RefSeqGene	NG_046964.1:g.52662AT[23]
GABRG1 RefSeqGene	NG_046964.1:g.52662AT[24]
GABRG1 RefSeqGene	NG_046964.1:g.52662AT[25]
GABRG1 RefSeqGene	NG_046964.1:g.52662AT[26]
GABRG1 RefSeqGene	NG_046964.1:g.52662AT[27]

Gene: GABRG1, gamma-aminobutyric acid type A receptor subunit gamma1 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
GABRG1 transcript	NM_173536.4:c.321+7582AT[… NM_173536.4:c.321+7582AT[5]	N/A	Intron Variant
GABRG1 transcript variant X1	XM_017007990.2:c.-67+2827… XM_017007990.2:c.-67+2827AT[5]	N/A	Intron 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	(AT)₂₁=	del(AT)₁₆	del(AT)₁₅	del(AT)₁₄	del(AT)₁₃	del(AT)₁₂	del(AT)₁₁	del(AT)₁₀	del(AT)₉	del(AT)₈	del(AT)₇	del(AT)₆	del(AT)₅	del(AT)₄	del(AT)₃	delATAT	delAT	dupAT	dupATAT	dup(AT)₃	dup(AT)₄	dup(AT)₅	dup(AT)₆
GRCh38.p14 chr 4	NC_000004.12:g.46076363_46076404=	NC_000004.12:g.46076363AT[5]	NC_000004.12:g.46076363AT[6]	NC_000004.12:g.46076363AT[7]	NC_000004.12:g.46076363AT[8]	NC_000004.12:g.46076363AT[9]	NC_000004.12:g.46076363AT[10]	NC_000004.12:g.46076363AT[11]	NC_000004.12:g.46076363AT[12]	NC_000004.12:g.46076363AT[13]	NC_000004.12:g.46076363AT[14]	NC_000004.12:g.46076363AT[15]	NC_000004.12:g.46076363AT[16]	NC_000004.12:g.46076363AT[17]	NC_000004.12:g.46076363AT[18]	NC_000004.12:g.46076363AT[19]	NC_000004.12:g.46076363AT[20]	NC_000004.12:g.46076363AT[22]	NC_000004.12:g.46076363AT[23]	NC_000004.12:g.46076363AT[24]	NC_000004.12:g.46076363AT[25]	NC_000004.12:g.46076363AT[26]	NC_000004.12:g.46076363AT[27]
GRCh37.p13 chr 4	NC_000004.11:g.46078380_46078421=	NC_000004.11:g.46078380AT[5]	NC_000004.11:g.46078380AT[6]	NC_000004.11:g.46078380AT[7]	NC_000004.11:g.46078380AT[8]	NC_000004.11:g.46078380AT[9]	NC_000004.11:g.46078380AT[10]	NC_000004.11:g.46078380AT[11]	NC_000004.11:g.46078380AT[12]	NC_000004.11:g.46078380AT[13]	NC_000004.11:g.46078380AT[14]	NC_000004.11:g.46078380AT[15]	NC_000004.11:g.46078380AT[16]	NC_000004.11:g.46078380AT[17]	NC_000004.11:g.46078380AT[18]	NC_000004.11:g.46078380AT[19]	NC_000004.11:g.46078380AT[20]	NC_000004.11:g.46078380AT[22]	NC_000004.11:g.46078380AT[23]	NC_000004.11:g.46078380AT[24]	NC_000004.11:g.46078380AT[25]	NC_000004.11:g.46078380AT[26]	NC_000004.11:g.46078380AT[27]
GABRG1 RefSeqGene	NG_046964.1:g.52662_52703=	NG_046964.1:g.52662AT[5]	NG_046964.1:g.52662AT[6]	NG_046964.1:g.52662AT[7]	NG_046964.1:g.52662AT[8]	NG_046964.1:g.52662AT[9]	NG_046964.1:g.52662AT[10]	NG_046964.1:g.52662AT[11]	NG_046964.1:g.52662AT[12]	NG_046964.1:g.52662AT[13]	NG_046964.1:g.52662AT[14]	NG_046964.1:g.52662AT[15]	NG_046964.1:g.52662AT[16]	NG_046964.1:g.52662AT[17]	NG_046964.1:g.52662AT[18]	NG_046964.1:g.52662AT[19]	NG_046964.1:g.52662AT[20]	NG_046964.1:g.52662AT[22]	NG_046964.1:g.52662AT[23]	NG_046964.1:g.52662AT[24]	NG_046964.1:g.52662AT[25]	NG_046964.1:g.52662AT[26]	NG_046964.1:g.52662AT[27]
GABRG1 transcript	NM_173536.3:c.321+7623=	NM_173536.3:c.321+7582AT[5]	NM_173536.3:c.321+7582AT[6]	NM_173536.3:c.321+7582AT[7]	NM_173536.3:c.321+7582AT[8]	NM_173536.3:c.321+7582AT[9]	NM_173536.3:c.321+7582AT[10]	NM_173536.3:c.321+7582AT[11]	NM_173536.3:c.321+7582AT[12]	NM_173536.3:c.321+7582AT[13]	NM_173536.3:c.321+7582AT[14]	NM_173536.3:c.321+7582AT[15]	NM_173536.3:c.321+7582AT[16]	NM_173536.3:c.321+7582AT[17]	NM_173536.3:c.321+7582AT[18]	NM_173536.3:c.321+7582AT[19]	NM_173536.3:c.321+7582AT[20]	NM_173536.3:c.321+7582AT[22]	NM_173536.3:c.321+7582AT[23]	NM_173536.3:c.321+7582AT[24]	NM_173536.3:c.321+7582AT[25]	NM_173536.3:c.321+7582AT[26]	NM_173536.3:c.321+7582AT[27]
GABRG1 transcript	NM_173536.4:c.321+7623=	NM_173536.4:c.321+7582AT[5]	NM_173536.4:c.321+7582AT[6]	NM_173536.4:c.321+7582AT[7]	NM_173536.4:c.321+7582AT[8]	NM_173536.4:c.321+7582AT[9]	NM_173536.4:c.321+7582AT[10]	NM_173536.4:c.321+7582AT[11]	NM_173536.4:c.321+7582AT[12]	NM_173536.4:c.321+7582AT[13]	NM_173536.4:c.321+7582AT[14]	NM_173536.4:c.321+7582AT[15]	NM_173536.4:c.321+7582AT[16]	NM_173536.4:c.321+7582AT[17]	NM_173536.4:c.321+7582AT[18]	NM_173536.4:c.321+7582AT[19]	NM_173536.4:c.321+7582AT[20]	NM_173536.4:c.321+7582AT[22]	NM_173536.4:c.321+7582AT[23]	NM_173536.4:c.321+7582AT[24]	NM_173536.4:c.321+7582AT[25]	NM_173536.4:c.321+7582AT[26]	NM_173536.4:c.321+7582AT[27]
GABRG1 transcript variant X1	XM_017007990.2:c.-67+2868=	XM_017007990.2:c.-67+2827AT[5]	XM_017007990.2:c.-67+2827AT[6]	XM_017007990.2:c.-67+2827AT[7]	XM_017007990.2:c.-67+2827AT[8]	XM_017007990.2:c.-67+2827AT[9]	XM_017007990.2:c.-67+2827AT[10]	XM_017007990.2:c.-67+2827AT[11]	XM_017007990.2:c.-67+2827AT[12]	XM_017007990.2:c.-67+2827AT[13]	XM_017007990.2:c.-67+2827AT[14]	XM_017007990.2:c.-67+2827AT[15]	XM_017007990.2:c.-67+2827AT[16]	XM_017007990.2:c.-67+2827AT[17]	XM_017007990.2:c.-67+2827AT[18]	XM_017007990.2:c.-67+2827AT[19]	XM_017007990.2:c.-67+2827AT[20]	XM_017007990.2:c.-67+2827AT[22]	XM_017007990.2:c.-67+2827AT[23]	XM_017007990.2:c.-67+2827AT[24]	XM_017007990.2:c.-67+2827AT[25]	XM_017007990.2:c.-67+2827AT[26]	XM_017007990.2:c.-67+2827AT[27]

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#.

54 SubSNP, 39 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	MCHAISSO	ss3065946420	Nov 08, 2017 (151)
2	EVA_DECODE	ss3711937862	Jul 13, 2019 (153)
3	EVA_DECODE	ss3711937863	Jul 13, 2019 (153)
4	EVA_DECODE	ss3711937864	Jul 13, 2019 (153)
5	EVA_DECODE	ss3711937865	Jul 13, 2019 (153)
6	EVA_DECODE	ss3711937866	Jul 13, 2019 (153)
7	EVA_DECODE	ss3711937867	Jul 13, 2019 (153)
8	ACPOP	ss3731098970	Jul 13, 2019 (153)
9	ACPOP	ss3731098972	Jul 13, 2019 (153)
10	ACPOP	ss3731098973	Jul 13, 2019 (153)
11	ACPOP	ss3731098974	Jul 13, 2019 (153)
12	ACPOP	ss3731098975	Jul 13, 2019 (153)
13	PACBIO	ss3784695226	Jul 13, 2019 (153)
14	PACBIO	ss3790155900	Jul 13, 2019 (153)
15	PACBIO	ss3795031137	Jul 13, 2019 (153)
16	KOGIC	ss3954017325	Apr 26, 2020 (154)
17	KOGIC	ss3954017326	Apr 26, 2020 (154)
18	KOGIC	ss3954017327	Apr 26, 2020 (154)
19	KOGIC	ss3954017328	Apr 26, 2020 (154)
20	GNOMAD	ss4095107242	Apr 26, 2021 (155)
21	GNOMAD	ss4095107243	Apr 26, 2021 (155)
22	GNOMAD	ss4095107244	Apr 26, 2021 (155)
23	GNOMAD	ss4095107245	Apr 26, 2021 (155)
24	GNOMAD	ss4095107246	Apr 26, 2021 (155)
25	GNOMAD	ss4095107247	Apr 26, 2021 (155)
26	GNOMAD	ss4095107250	Apr 26, 2021 (155)
27	GNOMAD	ss4095107251	Apr 26, 2021 (155)
28	GNOMAD	ss4095107252	Apr 26, 2021 (155)
29	GNOMAD	ss4095107253	Apr 26, 2021 (155)
30	GNOMAD	ss4095107254	Apr 26, 2021 (155)
31	GNOMAD	ss4095107255	Apr 26, 2021 (155)
32	GNOMAD	ss4095107256	Apr 26, 2021 (155)
33	GNOMAD	ss4095107257	Apr 26, 2021 (155)
34	GNOMAD	ss4095107258	Apr 26, 2021 (155)
35	GNOMAD	ss4095107259	Apr 26, 2021 (155)
36	GNOMAD	ss4095107260	Apr 26, 2021 (155)
37	GNOMAD	ss4095107261	Apr 26, 2021 (155)
38	GNOMAD	ss4095107262	Apr 26, 2021 (155)
39	GNOMAD	ss4095107263	Apr 26, 2021 (155)
40	GNOMAD	ss4095107264	Apr 26, 2021 (155)
41	TOMMO_GENOMICS	ss5165379013	Apr 26, 2021 (155)
42	TOMMO_GENOMICS	ss5165379014	Apr 26, 2021 (155)
43	TOMMO_GENOMICS	ss5165379015	Apr 26, 2021 (155)
44	TOMMO_GENOMICS	ss5165379016	Apr 26, 2021 (155)
45	1000G_HIGH_COVERAGE	ss5258977427	Oct 13, 2022 (156)
46	1000G_HIGH_COVERAGE	ss5258977428	Oct 13, 2022 (156)
47	1000G_HIGH_COVERAGE	ss5258977429	Oct 13, 2022 (156)
48	HUGCELL_USP	ss5457786210	Oct 13, 2022 (156)
49	HUGCELL_USP	ss5457786211	Oct 13, 2022 (156)
50	HUGCELL_USP	ss5457786212	Oct 13, 2022 (156)
51	TOMMO_GENOMICS	ss5699353365	Oct 13, 2022 (156)
52	TOMMO_GENOMICS	ss5699353366	Oct 13, 2022 (156)
53	TOMMO_GENOMICS	ss5699353367	Oct 13, 2022 (156)
54	TOMMO_GENOMICS	ss5699353369	Oct 13, 2022 (156)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 147840290 (NC_000004.12:46076362::AT 4056/72128) Row 147840291 (NC_000004.12:46076362::ATAT 602/73526) Row 147840292 (NC_000004.12:46076362::ATATAT 132/73890)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 147840290 (NC_000004.12:46076362::AT 4056/72128) Row 147840291 (NC_000004.12:46076362::ATAT 602/73526) Row 147840292 (NC_000004.12:46076362::ATATAT 132/73890)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 147840290 (NC_000004.12:46076362::AT 4056/72128) Row 147840291 (NC_000004.12:46076362::ATAT 602/73526) Row 147840292 (NC_000004.12:46076362::ATATAT 132/73890)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 147840290 (NC_000004.12:46076362::AT 4056/72128) Row 147840291 (NC_000004.12:46076362::ATAT 602/73526) Row 147840292 (NC_000004.12:46076362::ATATAT 132/73890)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 147840290 (NC_000004.12:46076362::AT 4056/72128) Row 147840291 (NC_000004.12:46076362::ATAT 602/73526) Row 147840292 (NC_000004.12:46076362::ATATAT 132/73890)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 147840290 (NC_000004.12:46076362::AT 4056/72128) Row 147840291 (NC_000004.12:46076362::ATAT 602/73526) Row 147840292 (NC_000004.12:46076362::ATATAT 132/73890)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 147840290 (NC_000004.12:46076362::AT 4056/72128) Row 147840291 (NC_000004.12:46076362::ATAT 602/73526) Row 147840292 (NC_000004.12:46076362::ATATAT 132/73890)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 147840290 (NC_000004.12:46076362::AT 4056/72128) Row 147840291 (NC_000004.12:46076362::ATAT 602/73526) Row 147840292 (NC_000004.12:46076362::ATATAT 132/73890)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 147840290 (NC_000004.12:46076362::AT 4056/72128) Row 147840291 (NC_000004.12:46076362::ATAT 602/73526) Row 147840292 (NC_000004.12:46076362::ATATAT 132/73890)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 147840290 (NC_000004.12:46076362::AT 4056/72128) Row 147840291 (NC_000004.12:46076362::ATAT 602/73526) Row 147840292 (NC_000004.12:46076362::ATATAT 132/73890)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 147840290 (NC_000004.12:46076362::AT 4056/72128) Row 147840291 (NC_000004.12:46076362::ATAT 602/73526) Row 147840292 (NC_000004.12:46076362::ATATAT 132/73890)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 147840290 (NC_000004.12:46076362::AT 4056/72128) Row 147840291 (NC_000004.12:46076362::ATAT 602/73526) Row 147840292 (NC_000004.12:46076362::ATATAT 132/73890)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 147840290 (NC_000004.12:46076362::AT 4056/72128) Row 147840291 (NC_000004.12:46076362::ATAT 602/73526) Row 147840292 (NC_000004.12:46076362::ATATAT 132/73890)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 147840290 (NC_000004.12:46076362::AT 4056/72128) Row 147840291 (NC_000004.12:46076362::ATAT 602/73526) Row 147840292 (NC_000004.12:46076362::ATATAT 132/73890)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 147840290 (NC_000004.12:46076362::AT 4056/72128) Row 147840291 (NC_000004.12:46076362::ATAT 602/73526) Row 147840292 (NC_000004.12:46076362::ATATAT 132/73890)...	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 147840290 (NC_000004.12:46076362::AT 4056/72128) Row 147840291 (NC_000004.12:46076362::ATAT 602/73526) Row 147840292 (NC_000004.12:46076362::ATATAT 132/73890)...	-	Apr 26, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 147840290 (NC_000004.12:46076362::AT 4056/72128) Row 147840291 (NC_000004.12:46076362::ATAT 602/73526) Row 147840292 (NC_000004.12:46076362::ATATAT 132/73890)...	-	Apr 26, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 147840290 (NC_000004.12:46076362::AT 4056/72128) Row 147840291 (NC_000004.12:46076362::ATAT 602/73526) Row 147840292 (NC_000004.12:46076362::ATATAT 132/73890)...	-	Apr 26, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 147840290 (NC_000004.12:46076362::AT 4056/72128) Row 147840291 (NC_000004.12:46076362::ATAT 602/73526) Row 147840292 (NC_000004.12:46076362::ATATAT 132/73890)...	-	Apr 26, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 147840290 (NC_000004.12:46076362::AT 4056/72128) Row 147840291 (NC_000004.12:46076362::ATAT 602/73526) Row 147840292 (NC_000004.12:46076362::ATATAT 132/73890)...	-	Apr 26, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 147840290 (NC_000004.12:46076362::AT 4056/72128) Row 147840291 (NC_000004.12:46076362::ATAT 602/73526) Row 147840292 (NC_000004.12:46076362::ATATAT 132/73890)...	-	Apr 26, 2021 (155)
76	Korean Genome Project Submission ignored due to conflicting rows: Row 10395326 (NC_000004.12:46076374:ATAT: 95/1684) Row 10395327 (NC_000004.12:46076378::AT 178/1684) Row 10395328 (NC_000004.12:46076376:AT: 112/1684)...	-	Apr 26, 2020 (154)
77	Korean Genome Project Submission ignored due to conflicting rows: Row 10395326 (NC_000004.12:46076374:ATAT: 95/1684) Row 10395327 (NC_000004.12:46076378::AT 178/1684) Row 10395328 (NC_000004.12:46076376:AT: 112/1684)...	-	Apr 26, 2020 (154)
78	Korean Genome Project Submission ignored due to conflicting rows: Row 10395326 (NC_000004.12:46076374:ATAT: 95/1684) Row 10395327 (NC_000004.12:46076378::AT 178/1684) Row 10395328 (NC_000004.12:46076376:AT: 112/1684)...	-	Apr 26, 2020 (154)
79	Korean Genome Project Submission ignored due to conflicting rows: Row 10395326 (NC_000004.12:46076374:ATAT: 95/1684) Row 10395327 (NC_000004.12:46076378::AT 178/1684) Row 10395328 (NC_000004.12:46076376:AT: 112/1684)...	-	Apr 26, 2020 (154)
80	Northern Sweden Submission ignored due to conflicting rows: Row 4383835 (NC_000004.11:46078379:AT: 66/568) Row 4383837 (NC_000004.11:46078379:ATAT: 14/568) Row 4383838 (NC_000004.11:46078379::AT 30/568)...	-	Jul 13, 2019 (153)
81	Northern Sweden Submission ignored due to conflicting rows: Row 4383835 (NC_000004.11:46078379:AT: 66/568) Row 4383837 (NC_000004.11:46078379:ATAT: 14/568) Row 4383838 (NC_000004.11:46078379::AT 30/568)...	-	Jul 13, 2019 (153)
82	Northern Sweden Submission ignored due to conflicting rows: Row 4383835 (NC_000004.11:46078379:AT: 66/568) Row 4383837 (NC_000004.11:46078379:ATAT: 14/568) Row 4383838 (NC_000004.11:46078379::AT 30/568)...	-	Jul 13, 2019 (153)
83	Northern Sweden Submission ignored due to conflicting rows: Row 4383835 (NC_000004.11:46078379:AT: 66/568) Row 4383837 (NC_000004.11:46078379:ATAT: 14/568) Row 4383838 (NC_000004.11:46078379::AT 30/568)...	-	Jul 13, 2019 (153)
84	Northern Sweden Submission ignored due to conflicting rows: Row 4383835 (NC_000004.11:46078379:AT: 66/568) Row 4383837 (NC_000004.11:46078379:ATAT: 14/568) Row 4383838 (NC_000004.11:46078379::AT 30/568)...	-	Jul 13, 2019 (153)
85	8.3KJPN Submission ignored due to conflicting rows: Row 23348320 (NC_000004.11:46078379:ATAT: 1490/16704) Row 23348321 (NC_000004.11:46078379::AT 3341/16704) Row 23348322 (NC_000004.11:46078379::ATAT 536/16704)...	-	Apr 26, 2021 (155)
86	8.3KJPN Submission ignored due to conflicting rows: Row 23348320 (NC_000004.11:46078379:ATAT: 1490/16704) Row 23348321 (NC_000004.11:46078379::AT 3341/16704) Row 23348322 (NC_000004.11:46078379::ATAT 536/16704)...	-	Apr 26, 2021 (155)
87	8.3KJPN Submission ignored due to conflicting rows: Row 23348320 (NC_000004.11:46078379:ATAT: 1490/16704) Row 23348321 (NC_000004.11:46078379::AT 3341/16704) Row 23348322 (NC_000004.11:46078379::ATAT 536/16704)...	-	Apr 26, 2021 (155)
88	8.3KJPN Submission ignored due to conflicting rows: Row 23348320 (NC_000004.11:46078379:ATAT: 1490/16704) Row 23348321 (NC_000004.11:46078379::AT 3341/16704) Row 23348322 (NC_000004.11:46078379::ATAT 536/16704)...	-	Apr 26, 2021 (155)
89	14KJPN Submission ignored due to conflicting rows: Row 33190469 (NC_000004.12:46076362:AT: 1415/28222) Row 33190470 (NC_000004.12:46076362::AT 5675/28222) Row 33190471 (NC_000004.12:46076362::ATAT 904/28222)...	-	Oct 13, 2022 (156)
90	14KJPN Submission ignored due to conflicting rows: Row 33190469 (NC_000004.12:46076362:AT: 1415/28222) Row 33190470 (NC_000004.12:46076362::AT 5675/28222) Row 33190471 (NC_000004.12:46076362::ATAT 904/28222)...	-	Oct 13, 2022 (156)
91	14KJPN Submission ignored due to conflicting rows: Row 33190469 (NC_000004.12:46076362:AT: 1415/28222) Row 33190470 (NC_000004.12:46076362::AT 5675/28222) Row 33190471 (NC_000004.12:46076362::ATAT 904/28222)...	-	Oct 13, 2022 (156)
92	14KJPN Submission ignored due to conflicting rows: Row 33190469 (NC_000004.12:46076362:AT: 1415/28222) Row 33190470 (NC_000004.12:46076362::AT 5675/28222) Row 33190471 (NC_000004.12:46076362::ATAT 904/28222)...	-	Oct 13, 2022 (156)
93	ALFA	NC_000004.12 - 46076363	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
7418394867	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATATATATATATATATAT:ATATATATAT	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATATATATATATATATAT:ATATATATAT	(self)
ss4095107264	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATATAT:	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATATATATATATATATAT:ATATATATATAT	(self)
7418394867	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATATATATATATATATAT:ATATATATATAT	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATATATATATATATATAT:ATATATATATAT	(self)
ss4095107263	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATAT:	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATAT	(self)
7418394867	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATAT	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATAT	(self)
ss4095107262	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATAT:	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATAT	(self)
7418394867	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATAT	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATAT	(self)
ss3711937867, ss4095107261	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATAT:	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATAT	(self)
7418394867	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATAT	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATAT	(self)
ss4095107260	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATAT:	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATAT	(self)
7418394867	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATAT	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATAT	(self)
ss4095107259	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATAT:	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATAT	(self)
7418394867	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATAT	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATAT	(self)
ss3711937866	NC_000004.12:46076366:ATATATATATAT… NC_000004.12:46076366:ATATATATATATATATATAT:	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATAT	(self)
ss4095107258	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATAT:	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATAT	(self)
7418394867	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATAT	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATAT	(self)
ss4095107257	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATAT:	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATAT	(self)
7418394867	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATAT	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATAT	(self)
ss4095107256	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATAT:	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATAT	(self)
7418394867	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATAT	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATAT	(self)
ss4095107255	NC_000004.12:46076362:ATATATATATAT:	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATAT	(self)
7418394867	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATAT	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATAT	(self)
ss4095107254	NC_000004.12:46076362:ATATATATAT:	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATAT	(self)
7418394867	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATAT	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATAT	(self)
ss4095107253	NC_000004.12:46076362:ATATATAT:	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATAT	(self)
7418394867	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATAT	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATAT	(self)
ss4095107252	NC_000004.12:46076362:ATATAT:	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATAT	(self)
7418394867	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATAT	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATAT	(self)
ss3954017328	NC_000004.12:46076372:ATATAT:	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATAT	(self)
ss3731098972, ss5165379013	NC_000004.11:46078379:ATAT:	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATAT	(self)
ss3065946420, ss4095107251, ss5258977427, ss5457786211, ss5699353369	NC_000004.12:46076362:ATAT:	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATAT	(self)
7418394867	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATAT	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATAT	(self)
ss3954017325	NC_000004.12:46076374:ATAT:	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATAT	(self)
ss3711937865	NC_000004.12:46076382:ATAT:	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATAT	(self)
ss3731098970, ss3784695226, ss3790155900, ss3795031137, ss5165379016	NC_000004.11:46078379:AT:	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATAT	(self)
ss4095107250, ss5258977428, ss5457786210, ss5699353365	NC_000004.12:46076362:AT:	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATAT	(self)
7418394867	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATAT	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATAT	(self)
ss3954017327	NC_000004.12:46076376:AT:	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATAT	(self)
ss3711937864	NC_000004.12:46076384:AT:	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATAT	(self)
ss3731098973, ss5165379014	NC_000004.11:46078379::AT	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATATAT	(self)
ss4095107242, ss5457786212, ss5699353366	NC_000004.12:46076362::AT	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATATAT	(self)
7418394867	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATATAT	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATATAT	(self)
ss3954017326	NC_000004.12:46076378::AT	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATATAT	(self)
ss3711937863	NC_000004.12:46076386::AT	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATATAT	(self)
ss3731098974, ss5165379015	NC_000004.11:46078379::ATAT	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATATATAT	(self)
ss4095107243, ss5258977429, ss5699353367	NC_000004.12:46076362::ATAT	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATATATAT	(self)
7418394867	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATATATAT	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATATATAT	(self)
ss3711937862	NC_000004.12:46076386::ATAT	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATATATAT	(self)
ss3731098975	NC_000004.11:46078379::ATATAT	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATATATATAT	(self)
ss4095107244	NC_000004.12:46076362::ATATAT	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATATATATAT	(self)
7418394867	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATATATATAT	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATATATATAT	(self)
ss4095107245	NC_000004.12:46076362::ATATATAT	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATATATATATAT	(self)
7418394867	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATATATATATAT	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATATATATATAT	(self)
ss4095107246	NC_000004.12:46076362::ATATATATAT	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATATATATATATAT	(self)
7418394867	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATATATATATATAT	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATATATATATATAT	(self)
ss4095107247	NC_000004.12:46076362::ATATATATATAT	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATATATATATATATAT	(self)
7418394867	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATATATATATATATAT	NC_000004.12:46076362:ATATATATATAT… NC_000004.12:46076362:ATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATATATATATATATAT	(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 rs1203391424

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
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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

rs1203391424