Name: rs71098461
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.

rs71098461

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr3:47190075-47190106 (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(T)₁₈ / del(T)₁₇ / del(T)₁₆ / d…
del(T)₁₈ / del(T)₁₇ / del(T)₁₆ / del(T)₁₅ / del(T)₁₄ / del(T)₁₃ / del(T)₁₂ / del(T)₁₁ / del(T)₁₀ / del(T)₉ / del(T)₈ / del(T)₇ / del(T)₆ / del(T)₅ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₅ / dup(T)₆ / dup(T)₉ / dup(T)₁₀ / dup(T)₁₁ / dup(T)₁₂ / dup(T)₁₃ / dup(T)₁₇ / dup(T)₂₉
Variation Type: Indel Insertion and Deletion
Frequency: del(T)₁₈=0.00000 (0/10546, ALFA)
del(T)₁₇=0.00000 (0/10546, ALFA)
del(T)₁₆=0.00000 (0/10546, ALFA) (+ 19 more)
del(T)₁₅=0.00000 (0/10546, ALFA)
del(T)₁₄=0.00000 (0/10546, ALFA)
del(T)₁₃=0.00000 (0/10546, ALFA)
del(T)₁₂=0.00000 (0/10546, ALFA)
del(T)₁₁=0.00000 (0/10546, ALFA)
del(T)₁₀=0.00000 (0/10546, ALFA)
del(T)₉=0.00000 (0/10546, ALFA)
del(T)₈=0.00000 (0/10546, ALFA)
del(T)₇=0.00000 (0/10546, ALFA)
del(T)₆=0.00000 (0/10546, ALFA)
del(T)₅=0.00000 (0/10546, ALFA)
del(T)₄=0.00000 (0/10546, ALFA)
delTTT=0.00000 (0/10546, ALFA)
delTT=0.00000 (0/10546, ALFA)
delT=0.00000 (0/10546, ALFA)
dupT=0.00000 (0/10546, ALFA)
dupTT=0.00000 (0/10546, ALFA)
dupTTT=0.00000 (0/10546, ALFA)
dup(T)₅=0.00000 (0/10546, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: KIF9-AS1 : 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	10546	TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.00000	TTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000	1.0	N/A
European	Sub	7124	TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
African	Sub	2130	TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
African Others	Sub	82	TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
African American	Sub	2048	TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
Asian	Sub	102	TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	N/A
East Asian	Sub	78	TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Other Asian	Sub	24	TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Latin American 1	Sub	136	TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	N/A
Latin American 2	Sub	550	TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	N/A
South Asian	Sub	88	TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Other	Sub	416	TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=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	10546	(T)₃₂=1.00000	del(T)₁₈=0.00000, del(T)₁₇=0.00000, del(T)₁₆=0.00000, del(T)₁₅=0.00000, del(T)₁₄=0.00000, del(T)₁₃=0.00000, del(T)₁₂=0.00000, del(T)₁₁=0.00000, del(T)₁₀=0.00000, del(T)₉=0.00000, del(T)₈=0.00000, del(T)₇=0.00000, del(T)₆=0.00000, del(T)₅=0.00000, del(T)₄=0.00000, delTTT=0.00000, delTT=0.00000, delT=0.00000, dupT=0.00000, dupTT=0.00000, dupTTT=0.00000, dup(T)₅=0.00000
Allele Frequency Aggregator	European	Sub	7124	(T)₃₂=1.0000	del(T)₁₈=0.0000, del(T)₁₇=0.0000, del(T)₁₆=0.0000, del(T)₁₅=0.0000, del(T)₁₄=0.0000, del(T)₁₃=0.0000, del(T)₁₂=0.0000, del(T)₁₁=0.0000, del(T)₁₀=0.0000, del(T)₉=0.0000, del(T)₈=0.0000, del(T)₇=0.0000, del(T)₆=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000, dupTTT=0.0000, dup(T)₅=0.0000
Allele Frequency Aggregator	African	Sub	2130	(T)₃₂=1.0000	del(T)₁₈=0.0000, del(T)₁₇=0.0000, del(T)₁₆=0.0000, del(T)₁₅=0.0000, del(T)₁₄=0.0000, del(T)₁₃=0.0000, del(T)₁₂=0.0000, del(T)₁₁=0.0000, del(T)₁₀=0.0000, del(T)₉=0.0000, del(T)₈=0.0000, del(T)₇=0.0000, del(T)₆=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000, dupTTT=0.0000, dup(T)₅=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	550	(T)₃₂=1.000	del(T)₁₈=0.000, del(T)₁₇=0.000, del(T)₁₆=0.000, del(T)₁₅=0.000, del(T)₁₄=0.000, del(T)₁₃=0.000, del(T)₁₂=0.000, del(T)₁₁=0.000, del(T)₁₀=0.000, del(T)₉=0.000, del(T)₈=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₅=0.000
Allele Frequency Aggregator	Other	Sub	416	(T)₃₂=1.000	del(T)₁₈=0.000, del(T)₁₇=0.000, del(T)₁₆=0.000, del(T)₁₅=0.000, del(T)₁₄=0.000, del(T)₁₃=0.000, del(T)₁₂=0.000, del(T)₁₁=0.000, del(T)₁₀=0.000, del(T)₉=0.000, del(T)₈=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₅=0.000
Allele Frequency Aggregator	Latin American 1	Sub	136	(T)₃₂=1.000	del(T)₁₈=0.000, del(T)₁₇=0.000, del(T)₁₆=0.000, del(T)₁₅=0.000, del(T)₁₄=0.000, del(T)₁₃=0.000, del(T)₁₂=0.000, del(T)₁₁=0.000, del(T)₁₀=0.000, del(T)₉=0.000, del(T)₈=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₅=0.000
Allele Frequency Aggregator	Asian	Sub	102	(T)₃₂=1.000	del(T)₁₈=0.000, del(T)₁₇=0.000, del(T)₁₆=0.000, del(T)₁₅=0.000, del(T)₁₄=0.000, del(T)₁₃=0.000, del(T)₁₂=0.000, del(T)₁₁=0.000, del(T)₁₀=0.000, del(T)₉=0.000, del(T)₈=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₅=0.000
Allele Frequency Aggregator	South Asian	Sub	88	(T)₃₂=1.00	del(T)₁₈=0.00, del(T)₁₇=0.00, del(T)₁₆=0.00, del(T)₁₅=0.00, del(T)₁₄=0.00, del(T)₁₃=0.00, del(T)₁₂=0.00, del(T)₁₁=0.00, del(T)₁₀=0.00, del(T)₉=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₅=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 3	NC_000003.12:g.47190089_47190106del
GRCh38.p14 chr 3	NC_000003.12:g.47190090_47190106del
GRCh38.p14 chr 3	NC_000003.12:g.47190091_47190106del
GRCh38.p14 chr 3	NC_000003.12:g.47190092_47190106del
GRCh38.p14 chr 3	NC_000003.12:g.47190093_47190106del
GRCh38.p14 chr 3	NC_000003.12:g.47190094_47190106del
GRCh38.p14 chr 3	NC_000003.12:g.47190095_47190106del
GRCh38.p14 chr 3	NC_000003.12:g.47190096_47190106del
GRCh38.p14 chr 3	NC_000003.12:g.47190097_47190106del
GRCh38.p14 chr 3	NC_000003.12:g.47190098_47190106del
GRCh38.p14 chr 3	NC_000003.12:g.47190099_47190106del
GRCh38.p14 chr 3	NC_000003.12:g.47190100_47190106del
GRCh38.p14 chr 3	NC_000003.12:g.47190101_47190106del
GRCh38.p14 chr 3	NC_000003.12:g.47190102_47190106del
GRCh38.p14 chr 3	NC_000003.12:g.47190103_47190106del
GRCh38.p14 chr 3	NC_000003.12:g.47190104_47190106del
GRCh38.p14 chr 3	NC_000003.12:g.47190105_47190106del
GRCh38.p14 chr 3	NC_000003.12:g.47190106del
GRCh38.p14 chr 3	NC_000003.12:g.47190106dup
GRCh38.p14 chr 3	NC_000003.12:g.47190105_47190106dup
GRCh38.p14 chr 3	NC_000003.12:g.47190104_47190106dup
GRCh38.p14 chr 3	NC_000003.12:g.47190102_47190106dup
GRCh38.p14 chr 3	NC_000003.12:g.47190101_47190106dup
GRCh38.p14 chr 3	NC_000003.12:g.47190098_47190106dup
GRCh38.p14 chr 3	NC_000003.12:g.47190097_47190106dup
GRCh38.p14 chr 3	NC_000003.12:g.47190096_47190106dup
GRCh38.p14 chr 3	NC_000003.12:g.47190095_47190106dup
GRCh38.p14 chr 3	NC_000003.12:g.47190094_47190106dup
GRCh38.p14 chr 3	NC_000003.12:g.47190090_47190106dup
GRCh38.p14 chr 3	NC_000003.12:g.47190078_47190106dup
GRCh37.p13 chr 3	NC_000003.11:g.47231579_47231596del
GRCh37.p13 chr 3	NC_000003.11:g.47231580_47231596del
GRCh37.p13 chr 3	NC_000003.11:g.47231581_47231596del
GRCh37.p13 chr 3	NC_000003.11:g.47231582_47231596del
GRCh37.p13 chr 3	NC_000003.11:g.47231583_47231596del
GRCh37.p13 chr 3	NC_000003.11:g.47231584_47231596del
GRCh37.p13 chr 3	NC_000003.11:g.47231585_47231596del
GRCh37.p13 chr 3	NC_000003.11:g.47231586_47231596del
GRCh37.p13 chr 3	NC_000003.11:g.47231587_47231596del
GRCh37.p13 chr 3	NC_000003.11:g.47231588_47231596del
GRCh37.p13 chr 3	NC_000003.11:g.47231589_47231596del
GRCh37.p13 chr 3	NC_000003.11:g.47231590_47231596del
GRCh37.p13 chr 3	NC_000003.11:g.47231591_47231596del
GRCh37.p13 chr 3	NC_000003.11:g.47231592_47231596del
GRCh37.p13 chr 3	NC_000003.11:g.47231593_47231596del
GRCh37.p13 chr 3	NC_000003.11:g.47231594_47231596del
GRCh37.p13 chr 3	NC_000003.11:g.47231595_47231596del
GRCh37.p13 chr 3	NC_000003.11:g.47231596del
GRCh37.p13 chr 3	NC_000003.11:g.47231596dup
GRCh37.p13 chr 3	NC_000003.11:g.47231595_47231596dup
GRCh37.p13 chr 3	NC_000003.11:g.47231594_47231596dup
GRCh37.p13 chr 3	NC_000003.11:g.47231592_47231596dup
GRCh37.p13 chr 3	NC_000003.11:g.47231591_47231596dup
GRCh37.p13 chr 3	NC_000003.11:g.47231588_47231596dup
GRCh37.p13 chr 3	NC_000003.11:g.47231587_47231596dup
GRCh37.p13 chr 3	NC_000003.11:g.47231586_47231596dup
GRCh37.p13 chr 3	NC_000003.11:g.47231585_47231596dup
GRCh37.p13 chr 3	NC_000003.11:g.47231584_47231596dup
GRCh37.p13 chr 3	NC_000003.11:g.47231580_47231596dup
GRCh37.p13 chr 3	NC_000003.11:g.47231568_47231596dup

Gene: KIF9-AS1, KIF9 antisense RNA 1 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
KIF9-AS1 transcript	NR_033373.1:n.	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	(T)₃₂=	del(T)₁₈	del(T)₁₇	del(T)₁₆	del(T)₁₅	del(T)₁₄	del(T)₁₃	del(T)₁₂	del(T)₁₁	del(T)₁₀	del(T)₉	del(T)₈	del(T)₇	del(T)₆	del(T)₅	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₅	dup(T)₆	dup(T)₉	dup(T)₁₀	dup(T)₁₁	dup(T)₁₂	dup(T)₁₃	dup(T)₁₇	dup(T)₂₉
GRCh38.p14 chr 3	NC_000003.12:g.47190075_47190106=	NC_000003.12:g.47190089_47190106del	NC_000003.12:g.47190090_47190106del	NC_000003.12:g.47190091_47190106del	NC_000003.12:g.47190092_47190106del	NC_000003.12:g.47190093_47190106del	NC_000003.12:g.47190094_47190106del	NC_000003.12:g.47190095_47190106del	NC_000003.12:g.47190096_47190106del	NC_000003.12:g.47190097_47190106del	NC_000003.12:g.47190098_47190106del	NC_000003.12:g.47190099_47190106del	NC_000003.12:g.47190100_47190106del	NC_000003.12:g.47190101_47190106del	NC_000003.12:g.47190102_47190106del	NC_000003.12:g.47190103_47190106del	NC_000003.12:g.47190104_47190106del	NC_000003.12:g.47190105_47190106del	NC_000003.12:g.47190106del	NC_000003.12:g.47190106dup	NC_000003.12:g.47190105_47190106dup	NC_000003.12:g.47190104_47190106dup	NC_000003.12:g.47190102_47190106dup	NC_000003.12:g.47190101_47190106dup	NC_000003.12:g.47190098_47190106dup	NC_000003.12:g.47190097_47190106dup	NC_000003.12:g.47190096_47190106dup	NC_000003.12:g.47190095_47190106dup	NC_000003.12:g.47190094_47190106dup	NC_000003.12:g.47190090_47190106dup	NC_000003.12:g.47190078_47190106dup
GRCh37.p13 chr 3	NC_000003.11:g.47231565_47231596=	NC_000003.11:g.47231579_47231596del	NC_000003.11:g.47231580_47231596del	NC_000003.11:g.47231581_47231596del	NC_000003.11:g.47231582_47231596del	NC_000003.11:g.47231583_47231596del	NC_000003.11:g.47231584_47231596del	NC_000003.11:g.47231585_47231596del	NC_000003.11:g.47231586_47231596del	NC_000003.11:g.47231587_47231596del	NC_000003.11:g.47231588_47231596del	NC_000003.11:g.47231589_47231596del	NC_000003.11:g.47231590_47231596del	NC_000003.11:g.47231591_47231596del	NC_000003.11:g.47231592_47231596del	NC_000003.11:g.47231593_47231596del	NC_000003.11:g.47231594_47231596del	NC_000003.11:g.47231595_47231596del	NC_000003.11:g.47231596del	NC_000003.11:g.47231596dup	NC_000003.11:g.47231595_47231596dup	NC_000003.11:g.47231594_47231596dup	NC_000003.11:g.47231592_47231596dup	NC_000003.11:g.47231591_47231596dup	NC_000003.11:g.47231588_47231596dup	NC_000003.11:g.47231587_47231596dup	NC_000003.11:g.47231586_47231596dup	NC_000003.11:g.47231585_47231596dup	NC_000003.11:g.47231584_47231596dup	NC_000003.11:g.47231580_47231596dup	NC_000003.11:g.47231568_47231596dup

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#.

34 SubSNP, 28 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HUMANGENOME_JCVI	ss95316438	Feb 13, 2009 (130)
2	EVA_DECODE	ss3709154599	Jul 13, 2019 (153)
3	EVA_DECODE	ss3709154600	Jul 13, 2019 (153)
4	EVA_DECODE	ss3709154601	Jul 13, 2019 (153)
5	EVA_DECODE	ss3709154602	Jul 13, 2019 (153)
6	EVA_DECODE	ss3709154603	Jul 13, 2019 (153)
7	EVA_DECODE	ss3709154604	Jul 13, 2019 (153)
8	GNOMAD	ss4070329188	Apr 26, 2021 (155)
9	GNOMAD	ss4070329210	Apr 26, 2021 (155)
10	GNOMAD	ss4070329211	Apr 26, 2021 (155)
11	GNOMAD	ss4070329213	Apr 26, 2021 (155)
12	GNOMAD	ss4070329214	Apr 26, 2021 (155)
13	GNOMAD	ss4070329215	Apr 26, 2021 (155)
14	GNOMAD	ss4070329216	Apr 26, 2021 (155)
15	GNOMAD	ss4070329217	Apr 26, 2021 (155)
16	GNOMAD	ss4070329218	Apr 26, 2021 (155)
17	GNOMAD	ss4070329219	Apr 26, 2021 (155)
18	GNOMAD	ss4070329220	Apr 26, 2021 (155)
19	GNOMAD	ss4070329221	Apr 26, 2021 (155)
20	GNOMAD	ss4070329222	Apr 26, 2021 (155)
21	GNOMAD	ss4070329223	Apr 26, 2021 (155)
22	GNOMAD	ss4070329224	Apr 26, 2021 (155)
23	GNOMAD	ss4070329225	Apr 26, 2021 (155)
24	GNOMAD	ss4070329226	Apr 26, 2021 (155)
25	GNOMAD	ss4070329227	Apr 26, 2021 (155)
26	GNOMAD	ss4070329228	Apr 26, 2021 (155)
27	GNOMAD	ss4070329229	Apr 26, 2021 (155)
28	GNOMAD	ss4070329230	Apr 26, 2021 (155)
29	GNOMAD	ss4070329231	Apr 26, 2021 (155)
30	GNOMAD	ss4070329232	Apr 26, 2021 (155)
31	TOMMO_GENOMICS	ss5690558358	Oct 12, 2022 (156)
32	TOMMO_GENOMICS	ss5690558359	Oct 12, 2022 (156)
33	TOMMO_GENOMICS	ss5690558361	Oct 12, 2022 (156)
34	TOMMO_GENOMICS	ss5690558362	Oct 12, 2022 (156)
35	gnomAD - Genomes Submission ignored due to conflicting rows: Row 106558628 (NC_000003.12:47190074::T 87/10998) Row 106558650 (NC_000003.12:47190074::TT 292/10980) Row 106558651 (NC_000003.12:47190074::TTT 86/10956)...	-	Apr 26, 2021 (155)
36	gnomAD - Genomes Submission ignored due to conflicting rows: Row 106558628 (NC_000003.12:47190074::T 87/10998) Row 106558650 (NC_000003.12:47190074::TT 292/10980) Row 106558651 (NC_000003.12:47190074::TTT 86/10956)...	-	Apr 26, 2021 (155)
37	gnomAD - Genomes Submission ignored due to conflicting rows: Row 106558628 (NC_000003.12:47190074::T 87/10998) Row 106558650 (NC_000003.12:47190074::TT 292/10980) Row 106558651 (NC_000003.12:47190074::TTT 86/10956)...	-	Apr 26, 2021 (155)
38	gnomAD - Genomes Submission ignored due to conflicting rows: Row 106558628 (NC_000003.12:47190074::T 87/10998) Row 106558650 (NC_000003.12:47190074::TT 292/10980) Row 106558651 (NC_000003.12:47190074::TTT 86/10956)...	-	Apr 26, 2021 (155)
39	gnomAD - Genomes Submission ignored due to conflicting rows: Row 106558628 (NC_000003.12:47190074::T 87/10998) Row 106558650 (NC_000003.12:47190074::TT 292/10980) Row 106558651 (NC_000003.12:47190074::TTT 86/10956)...	-	Apr 26, 2021 (155)
40	gnomAD - Genomes Submission ignored due to conflicting rows: Row 106558628 (NC_000003.12:47190074::T 87/10998) Row 106558650 (NC_000003.12:47190074::TT 292/10980) Row 106558651 (NC_000003.12:47190074::TTT 86/10956)...	-	Apr 26, 2021 (155)
41	gnomAD - Genomes Submission ignored due to conflicting rows: Row 106558628 (NC_000003.12:47190074::T 87/10998) Row 106558650 (NC_000003.12:47190074::TT 292/10980) Row 106558651 (NC_000003.12:47190074::TTT 86/10956)...	-	Apr 26, 2021 (155)
42	gnomAD - Genomes Submission ignored due to conflicting rows: Row 106558628 (NC_000003.12:47190074::T 87/10998) Row 106558650 (NC_000003.12:47190074::TT 292/10980) Row 106558651 (NC_000003.12:47190074::TTT 86/10956)...	-	Apr 26, 2021 (155)
43	gnomAD - Genomes Submission ignored due to conflicting rows: Row 106558628 (NC_000003.12:47190074::T 87/10998) Row 106558650 (NC_000003.12:47190074::TT 292/10980) Row 106558651 (NC_000003.12:47190074::TTT 86/10956)...	-	Apr 26, 2021 (155)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 106558628 (NC_000003.12:47190074::T 87/10998) Row 106558650 (NC_000003.12:47190074::TT 292/10980) Row 106558651 (NC_000003.12:47190074::TTT 86/10956)...	-	Apr 26, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 106558628 (NC_000003.12:47190074::T 87/10998) Row 106558650 (NC_000003.12:47190074::TT 292/10980) Row 106558651 (NC_000003.12:47190074::TTT 86/10956)...	-	Apr 26, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 106558628 (NC_000003.12:47190074::T 87/10998) Row 106558650 (NC_000003.12:47190074::TT 292/10980) Row 106558651 (NC_000003.12:47190074::TTT 86/10956)...	-	Apr 26, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 106558628 (NC_000003.12:47190074::T 87/10998) Row 106558650 (NC_000003.12:47190074::TT 292/10980) Row 106558651 (NC_000003.12:47190074::TTT 86/10956)...	-	Apr 26, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 106558628 (NC_000003.12:47190074::T 87/10998) Row 106558650 (NC_000003.12:47190074::TT 292/10980) Row 106558651 (NC_000003.12:47190074::TTT 86/10956)...	-	Apr 26, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 106558628 (NC_000003.12:47190074::T 87/10998) Row 106558650 (NC_000003.12:47190074::TT 292/10980) Row 106558651 (NC_000003.12:47190074::TTT 86/10956)...	-	Apr 26, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 106558628 (NC_000003.12:47190074::T 87/10998) Row 106558650 (NC_000003.12:47190074::TT 292/10980) Row 106558651 (NC_000003.12:47190074::TTT 86/10956)...	-	Apr 26, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 106558628 (NC_000003.12:47190074::T 87/10998) Row 106558650 (NC_000003.12:47190074::TT 292/10980) Row 106558651 (NC_000003.12:47190074::TTT 86/10956)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 106558628 (NC_000003.12:47190074::T 87/10998) Row 106558650 (NC_000003.12:47190074::TT 292/10980) Row 106558651 (NC_000003.12:47190074::TTT 86/10956)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 106558628 (NC_000003.12:47190074::T 87/10998) Row 106558650 (NC_000003.12:47190074::TT 292/10980) Row 106558651 (NC_000003.12:47190074::TTT 86/10956)...	-	Apr 26, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 106558628 (NC_000003.12:47190074::T 87/10998) Row 106558650 (NC_000003.12:47190074::TT 292/10980) Row 106558651 (NC_000003.12:47190074::TTT 86/10956)...	-	Apr 26, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 106558628 (NC_000003.12:47190074::T 87/10998) Row 106558650 (NC_000003.12:47190074::TT 292/10980) Row 106558651 (NC_000003.12:47190074::TTT 86/10956)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 106558628 (NC_000003.12:47190074::T 87/10998) Row 106558650 (NC_000003.12:47190074::TT 292/10980) Row 106558651 (NC_000003.12:47190074::TTT 86/10956)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 106558628 (NC_000003.12:47190074::T 87/10998) Row 106558650 (NC_000003.12:47190074::TT 292/10980) Row 106558651 (NC_000003.12:47190074::TTT 86/10956)...	-	Apr 26, 2021 (155)
58	14KJPN Submission ignored due to conflicting rows: Row 24395462 (NC_000003.12:47190074:TTTTTTTTTTTTTTTT: 171/22812) Row 24395463 (NC_000003.12:47190074::T 650/22812) Row 24395465 (NC_000003.12:47190074::TTT 422/22812)...	-	Oct 12, 2022 (156)
59	14KJPN Submission ignored due to conflicting rows: Row 24395462 (NC_000003.12:47190074:TTTTTTTTTTTTTTTT: 171/22812) Row 24395463 (NC_000003.12:47190074::T 650/22812) Row 24395465 (NC_000003.12:47190074::TTT 422/22812)...	-	Oct 12, 2022 (156)
60	14KJPN Submission ignored due to conflicting rows: Row 24395462 (NC_000003.12:47190074:TTTTTTTTTTTTTTTT: 171/22812) Row 24395463 (NC_000003.12:47190074::T 650/22812) Row 24395465 (NC_000003.12:47190074::TTT 422/22812)...	-	Oct 12, 2022 (156)
61	14KJPN Submission ignored due to conflicting rows: Row 24395462 (NC_000003.12:47190074:TTTTTTTTTTTTTTTT: 171/22812) Row 24395463 (NC_000003.12:47190074::T 650/22812) Row 24395465 (NC_000003.12:47190074::TTT 422/22812)...	-	Oct 12, 2022 (156)
62	ALFA	NC_000003.12 - 47190075	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).

Associated ID	History Updated (Build)
rs72159092	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss3709154599, ss4070329232	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTTTTT:	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
6787294365	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
6787294365	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3709154600	NC_000003.12:47190075:TTTTTTTTTTTT… NC_000003.12:47190075:TTTTTTTTTTTTTTTTT:	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4070329231, ss5690558358	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTTT:	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
6787294365	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3709154601	NC_000003.12:47190076:TTTTTTTTTTTT… NC_000003.12:47190076:TTTTTTTTTTTTTTTT:	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4070329230	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTT:	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
6787294365	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss3709154602	NC_000003.12:47190077:TTTTTTTTTTTT… NC_000003.12:47190077:TTTTTTTTTTTTTTT:	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
6787294365	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4070329229	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTT:	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
6787294365	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4070329228	NC_000003.12:47190074:TTTTTTTTTTTT:	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
6787294365	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4070329227	NC_000003.12:47190074:TTTTTTTTTTT:	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
6787294365	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
6787294365	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4070329226	NC_000003.12:47190074:TTTTTTTTT:	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
6787294365	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
6787294365	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
6787294365	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
6787294365	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4070329225	NC_000003.12:47190074:TTTTT:	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
6787294365	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4070329224	NC_000003.12:47190074:TTTT:	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
6787294365	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4070329223	NC_000003.12:47190074:TTT:	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
6787294365	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4070329222	NC_000003.12:47190074:TT:	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
6787294365	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
6787294365	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4070329188, ss5690558359	NC_000003.12:47190074::T	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
6787294365	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3709154603	NC_000003.12:47190092::T	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss95316438	NT_022517.18:47171596::T	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4070329210, ss5690558362	NC_000003.12:47190074::TT	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
6787294365	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4070329211, ss5690558361	NC_000003.12:47190074::TTT	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
6787294365	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4070329213	NC_000003.12:47190074::TTTTT	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
6787294365	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3709154604	NC_000003.12:47190092::TTTTT	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4070329214	NC_000003.12:47190074::TTTTTT	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4070329215	NC_000003.12:47190074::TTTTTTTTT	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4070329216	NC_000003.12:47190074::TTTTTTTTTT	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4070329217	NC_000003.12:47190074::TTTTTTTTTTT	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4070329218	NC_000003.12:47190074::TTTTTTTTTTTT	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4070329219	NC_000003.12:47190074::TTTTTTTTTTT… NC_000003.12:47190074::TTTTTTTTTTTTT	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4070329220	NC_000003.12:47190074::TTTTTTTTTTT… NC_000003.12:47190074::TTTTTTTTTTTTTTTTT	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4070329221	NC_000003.12:47190074::TTTTTTTTTTT… NC_000003.12:47190074::TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI
ss3389436047	NC_000003.12:47190074:T:	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
ss3389436052	NC_000003.12:47190074:TTTTTT:	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT
ss3389436053	NC_000003.12:47190074:TTTTTTT:	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT
ss3389436054	NC_000003.12:47190074:TTTTTTTT:	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT
ss3389436056	NC_000003.12:47190074:TTTTTTTTTT:	NC_000003.12:47190074:TTTTTTTTTTTT… NC_000003.12:47190074:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT

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

No publications for rs71098461

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.

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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs71098461