Name: rs749424799
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.

rs749424799

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr19:21162145-21162185 (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(GT)₁₅ / del(GT)₉ / del(GT)₈ / …
del(GT)₁₅ / del(GT)₉ / del(GT)₈ / del(GT)₇ / del(GT)₆ / del(GT)₅ / del(GT)₄ / del(GT)₃ / delGTGT / delGT / dupGT / dupGTGT / dup(GT)₃ / dup(GT)₄ / dup(GT)₅ / dup(GT)₆ / dup(GT)₈
Variation Type: Indel Insertion and Deletion
Frequency: del(GT)₁₅=0.000004 (1/264690, TOPMED)
del(GT)₁₅=0.0000 (0/7472, ALFA)
del(GT)₉=0.0000 (0/7472, ALFA) (+ 15 more)
del(GT)₈=0.0000 (0/7472, ALFA)
del(GT)₇=0.0000 (0/7472, ALFA)
del(GT)₆=0.0000 (0/7472, ALFA)
del(GT)₅=0.0000 (0/7472, ALFA)
del(GT)₄=0.0000 (0/7472, ALFA)
del(GT)₃=0.0000 (0/7472, ALFA)
delGTGT=0.0000 (0/7472, ALFA)
delGT=0.0000 (0/7472, ALFA)
dupGT=0.0000 (0/7472, ALFA)
dupGTGT=0.0000 (0/7472, ALFA)
dup(GT)₃=0.0000 (0/7472, ALFA)
dup(GT)₄=0.0000 (0/7472, ALFA)
dup(GT)₅=0.0000 (0/7472, ALFA)
dup(GT)₆=0.0000 (0/7472, ALFA)
delGTGT=0.0789 (304/3854, ALSPAC)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: ZNF431 : 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	7472	TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=1.0000	TGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000	1.0	N/A
European	Sub	5430	TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=1.0000	TGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000	1.0	N/A
African	Sub	1242	TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=1.0000	TGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000	1.0	N/A
African Others	Sub	40	TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=1.00	TGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00	1.0	N/A
African American	Sub	1202	TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=1.0000	TGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000	1.0	N/A
Asian	Sub	84	TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=1.00	TGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00	1.0	N/A
East Asian	Sub	64	TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=1.00	TGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00	1.0	N/A
Other Asian	Sub	20	TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=1.00	TGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00	1.0	N/A
Latin American 1	Sub	86	TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=1.00	TGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00	1.0	N/A
Latin American 2	Sub	308	TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=1.000	TGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000	1.0	N/A
South Asian	Sub	70	TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=1.00	TGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00	1.0	N/A
Other	Sub	252	TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=1.000	TGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=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").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
TopMed	Global	Study-wide	264690	(TG)₂₀T=0.999996	del(GT)₁₅=0.000004
Allele Frequency Aggregator	Total	Global	7472	(TG)₂₀T=1.0000	del(GT)₁₅=0.0000, del(GT)₉=0.0000, del(GT)₈=0.0000, del(GT)₇=0.0000, del(GT)₆=0.0000, del(GT)₅=0.0000, del(GT)₄=0.0000, del(GT)₃=0.0000, delGTGT=0.0000, delGT=0.0000, dupGT=0.0000, dupGTGT=0.0000, dup(GT)₃=0.0000, dup(GT)₄=0.0000, dup(GT)₅=0.0000, dup(GT)₆=0.0000
Allele Frequency Aggregator	European	Sub	5430	(TG)₂₀T=1.0000	del(GT)₁₅=0.0000, del(GT)₉=0.0000, del(GT)₈=0.0000, del(GT)₇=0.0000, del(GT)₆=0.0000, del(GT)₅=0.0000, del(GT)₄=0.0000, del(GT)₃=0.0000, delGTGT=0.0000, delGT=0.0000, dupGT=0.0000, dupGTGT=0.0000, dup(GT)₃=0.0000, dup(GT)₄=0.0000, dup(GT)₅=0.0000, dup(GT)₆=0.0000
Allele Frequency Aggregator	African	Sub	1242	(TG)₂₀T=1.0000	del(GT)₁₅=0.0000, del(GT)₉=0.0000, del(GT)₈=0.0000, del(GT)₇=0.0000, del(GT)₆=0.0000, del(GT)₅=0.0000, del(GT)₄=0.0000, del(GT)₃=0.0000, delGTGT=0.0000, delGT=0.0000, dupGT=0.0000, dupGTGT=0.0000, dup(GT)₃=0.0000, dup(GT)₄=0.0000, dup(GT)₅=0.0000, dup(GT)₆=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	308	(TG)₂₀T=1.000	del(GT)₁₅=0.000, del(GT)₉=0.000, del(GT)₈=0.000, del(GT)₇=0.000, del(GT)₆=0.000, del(GT)₅=0.000, del(GT)₄=0.000, del(GT)₃=0.000, delGTGT=0.000, delGT=0.000, dupGT=0.000, dupGTGT=0.000, dup(GT)₃=0.000, dup(GT)₄=0.000, dup(GT)₅=0.000, dup(GT)₆=0.000
Allele Frequency Aggregator	Other	Sub	252	(TG)₂₀T=1.000	del(GT)₁₅=0.000, del(GT)₉=0.000, del(GT)₈=0.000, del(GT)₇=0.000, del(GT)₆=0.000, del(GT)₅=0.000, del(GT)₄=0.000, del(GT)₃=0.000, delGTGT=0.000, delGT=0.000, dupGT=0.000, dupGTGT=0.000, dup(GT)₃=0.000, dup(GT)₄=0.000, dup(GT)₅=0.000, dup(GT)₆=0.000
Allele Frequency Aggregator	Latin American 1	Sub	86	(TG)₂₀T=1.00	del(GT)₁₅=0.00, del(GT)₉=0.00, del(GT)₈=0.00, del(GT)₇=0.00, del(GT)₆=0.00, del(GT)₅=0.00, del(GT)₄=0.00, del(GT)₃=0.00, delGTGT=0.00, delGT=0.00, dupGT=0.00, dupGTGT=0.00, dup(GT)₃=0.00, dup(GT)₄=0.00, dup(GT)₅=0.00, dup(GT)₆=0.00
Allele Frequency Aggregator	Asian	Sub	84	(TG)₂₀T=1.00	del(GT)₁₅=0.00, del(GT)₉=0.00, del(GT)₈=0.00, del(GT)₇=0.00, del(GT)₆=0.00, del(GT)₅=0.00, del(GT)₄=0.00, del(GT)₃=0.00, delGTGT=0.00, delGT=0.00, dupGT=0.00, dupGTGT=0.00, dup(GT)₃=0.00, dup(GT)₄=0.00, dup(GT)₅=0.00, dup(GT)₆=0.00
Allele Frequency Aggregator	South Asian	Sub	70	(TG)₂₀T=1.00	del(GT)₁₅=0.00, del(GT)₉=0.00, del(GT)₈=0.00, del(GT)₇=0.00, del(GT)₆=0.00, del(GT)₅=0.00, del(GT)₄=0.00, del(GT)₃=0.00, delGTGT=0.00, delGT=0.00, dupGT=0.00, dupGTGT=0.00, dup(GT)₃=0.00, dup(GT)₄=0.00, dup(GT)₅=0.00, dup(GT)₆=0.00
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	(TG)₂₀T=0.9211	delGTGT=0.0789

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 19	NC_000019.10:g.21162146GT[5]
GRCh38.p14 chr 19	NC_000019.10:g.21162146GT[11]
GRCh38.p14 chr 19	NC_000019.10:g.21162146GT[12]
GRCh38.p14 chr 19	NC_000019.10:g.21162146GT[13]
GRCh38.p14 chr 19	NC_000019.10:g.21162146GT[14]
GRCh38.p14 chr 19	NC_000019.10:g.21162146GT[15]
GRCh38.p14 chr 19	NC_000019.10:g.21162146GT[16]
GRCh38.p14 chr 19	NC_000019.10:g.21162146GT[17]
GRCh38.p14 chr 19	NC_000019.10:g.21162146GT[18]
GRCh38.p14 chr 19	NC_000019.10:g.21162146GT[19]
GRCh38.p14 chr 19	NC_000019.10:g.21162146GT[21]
GRCh38.p14 chr 19	NC_000019.10:g.21162146GT[22]
GRCh38.p14 chr 19	NC_000019.10:g.21162146GT[23]
GRCh38.p14 chr 19	NC_000019.10:g.21162146GT[24]
GRCh38.p14 chr 19	NC_000019.10:g.21162146GT[25]
GRCh38.p14 chr 19	NC_000019.10:g.21162146GT[26]
GRCh38.p14 chr 19	NC_000019.10:g.21162146GT[28]
GRCh37.p13 chr 19	NC_000019.9:g.21344949GT[5]
GRCh37.p13 chr 19	NC_000019.9:g.21344949GT[11]
GRCh37.p13 chr 19	NC_000019.9:g.21344949GT[12]
GRCh37.p13 chr 19	NC_000019.9:g.21344949GT[13]
GRCh37.p13 chr 19	NC_000019.9:g.21344949GT[14]
GRCh37.p13 chr 19	NC_000019.9:g.21344949GT[15]
GRCh37.p13 chr 19	NC_000019.9:g.21344949GT[16]
GRCh37.p13 chr 19	NC_000019.9:g.21344949GT[17]
GRCh37.p13 chr 19	NC_000019.9:g.21344949GT[18]
GRCh37.p13 chr 19	NC_000019.9:g.21344949GT[19]
GRCh37.p13 chr 19	NC_000019.9:g.21344949GT[21]
GRCh37.p13 chr 19	NC_000019.9:g.21344949GT[22]
GRCh37.p13 chr 19	NC_000019.9:g.21344949GT[23]
GRCh37.p13 chr 19	NC_000019.9:g.21344949GT[24]
GRCh37.p13 chr 19	NC_000019.9:g.21344949GT[25]
GRCh37.p13 chr 19	NC_000019.9:g.21344949GT[26]
GRCh37.p13 chr 19	NC_000019.9:g.21344949GT[28]
ZNF431 RefSeqGene	NG_051229.1:g.25138GT[5]
ZNF431 RefSeqGene	NG_051229.1:g.25138GT[11]
ZNF431 RefSeqGene	NG_051229.1:g.25138GT[12]
ZNF431 RefSeqGene	NG_051229.1:g.25138GT[13]
ZNF431 RefSeqGene	NG_051229.1:g.25138GT[14]
ZNF431 RefSeqGene	NG_051229.1:g.25138GT[15]
ZNF431 RefSeqGene	NG_051229.1:g.25138GT[16]
ZNF431 RefSeqGene	NG_051229.1:g.25138GT[17]
ZNF431 RefSeqGene	NG_051229.1:g.25138GT[18]
ZNF431 RefSeqGene	NG_051229.1:g.25138GT[19]
ZNF431 RefSeqGene	NG_051229.1:g.25138GT[21]
ZNF431 RefSeqGene	NG_051229.1:g.25138GT[22]
ZNF431 RefSeqGene	NG_051229.1:g.25138GT[23]
ZNF431 RefSeqGene	NG_051229.1:g.25138GT[24]
ZNF431 RefSeqGene	NG_051229.1:g.25138GT[25]
ZNF431 RefSeqGene	NG_051229.1:g.25138GT[26]
ZNF431 RefSeqGene	NG_051229.1:g.25138GT[28]

Gene: ZNF431, zinc finger protein 431 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
ZNF431 transcript variant 1	NM_001319124.2:c.97-4190T… NM_001319124.2:c.97-4190TG[5]	N/A	Intron Variant
ZNF431 transcript variant 3	NM_001319126.2:c.-199-419… NM_001319126.2:c.-199-4190TG[5]	N/A	Intron Variant
ZNF431 transcript variant 4	NM_001319127.2:c.-305-419… NM_001319127.2:c.-305-4190TG[5]	N/A	Intron Variant
ZNF431 transcript variant 2	NM_133473.4:c.97-4190TG[5]	N/A	Intron Variant
ZNF431 transcript variant 5	NR_138052.2:n.	N/A	Intron Variant
ZNF431 transcript variant 6	NR_138053.2:n.	N/A	Intron Variant
ZNF431 transcript variant X3	XR_001753620.2:n.	N/A	Intron Variant
ZNF431 transcript variant X1	XR_007066664.1:n.	N/A	Intron Variant
ZNF431 transcript variant X2	XR_007066665.1:n.	N/A	Intron Variant
ZNF431 transcript variant X4	XR_007066666.1:n.	N/A	Intron Variant
ZNF431 transcript variant X5	XR_007066667.1:n.	N/A	Intron Variant
ZNF431 transcript variant X6	XR_007066668.1:n.	N/A	Intron Variant
ZNF431 transcript variant X7	XR_007066669.1:n.	N/A	Intron Variant
ZNF431 transcript variant X8	XR_007066670.1: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	(TG)₂₀T=	del(GT)₁₅	del(GT)₉	del(GT)₈	del(GT)₇	del(GT)₆	del(GT)₅	del(GT)₄	del(GT)₃	delGTGT	delGT	dupGT	dupGTGT	dup(GT)₃	dup(GT)₄	dup(GT)₅	dup(GT)₆	dup(GT)₈
GRCh38.p14 chr 19	NC_000019.10:g.21162145_21162185=	NC_000019.10:g.21162146GT[5]	NC_000019.10:g.21162146GT[11]	NC_000019.10:g.21162146GT[12]	NC_000019.10:g.21162146GT[13]	NC_000019.10:g.21162146GT[14]	NC_000019.10:g.21162146GT[15]	NC_000019.10:g.21162146GT[16]	NC_000019.10:g.21162146GT[17]	NC_000019.10:g.21162146GT[18]	NC_000019.10:g.21162146GT[19]	NC_000019.10:g.21162146GT[21]	NC_000019.10:g.21162146GT[22]	NC_000019.10:g.21162146GT[23]	NC_000019.10:g.21162146GT[24]	NC_000019.10:g.21162146GT[25]	NC_000019.10:g.21162146GT[26]	NC_000019.10:g.21162146GT[28]
GRCh37.p13 chr 19	NC_000019.9:g.21344948_21344988=	NC_000019.9:g.21344949GT[5]	NC_000019.9:g.21344949GT[11]	NC_000019.9:g.21344949GT[12]	NC_000019.9:g.21344949GT[13]	NC_000019.9:g.21344949GT[14]	NC_000019.9:g.21344949GT[15]	NC_000019.9:g.21344949GT[16]	NC_000019.9:g.21344949GT[17]	NC_000019.9:g.21344949GT[18]	NC_000019.9:g.21344949GT[19]	NC_000019.9:g.21344949GT[21]	NC_000019.9:g.21344949GT[22]	NC_000019.9:g.21344949GT[23]	NC_000019.9:g.21344949GT[24]	NC_000019.9:g.21344949GT[25]	NC_000019.9:g.21344949GT[26]	NC_000019.9:g.21344949GT[28]
ZNF431 RefSeqGene	NG_051229.1:g.25137_25177=	NG_051229.1:g.25138GT[5]	NG_051229.1:g.25138GT[11]	NG_051229.1:g.25138GT[12]	NG_051229.1:g.25138GT[13]	NG_051229.1:g.25138GT[14]	NG_051229.1:g.25138GT[15]	NG_051229.1:g.25138GT[16]	NG_051229.1:g.25138GT[17]	NG_051229.1:g.25138GT[18]	NG_051229.1:g.25138GT[19]	NG_051229.1:g.25138GT[21]	NG_051229.1:g.25138GT[22]	NG_051229.1:g.25138GT[23]	NG_051229.1:g.25138GT[24]	NG_051229.1:g.25138GT[25]	NG_051229.1:g.25138GT[26]	NG_051229.1:g.25138GT[28]
ZNF431 transcript variant 1	NM_001319124.2:c.97-4190=	NM_001319124.2:c.97-4190TG[5]	NM_001319124.2:c.97-4190TG[11]	NM_001319124.2:c.97-4190TG[12]	NM_001319124.2:c.97-4190TG[13]	NM_001319124.2:c.97-4190TG[14]	NM_001319124.2:c.97-4190TG[15]	NM_001319124.2:c.97-4190TG[16]	NM_001319124.2:c.97-4190TG[17]	NM_001319124.2:c.97-4190TG[18]	NM_001319124.2:c.97-4190TG[19]	NM_001319124.2:c.97-4190TG[21]	NM_001319124.2:c.97-4190TG[22]	NM_001319124.2:c.97-4190TG[23]	NM_001319124.2:c.97-4190TG[24]	NM_001319124.2:c.97-4190TG[25]	NM_001319124.2:c.97-4190TG[26]	NM_001319124.2:c.97-4190TG[28]
ZNF431 transcript variant 3	NM_001319126.2:c.-199-4190=	NM_001319126.2:c.-199-4190TG[5]	NM_001319126.2:c.-199-4190TG[11]	NM_001319126.2:c.-199-4190TG[12]	NM_001319126.2:c.-199-4190TG[13]	NM_001319126.2:c.-199-4190TG[14]	NM_001319126.2:c.-199-4190TG[15]	NM_001319126.2:c.-199-4190TG[16]	NM_001319126.2:c.-199-4190TG[17]	NM_001319126.2:c.-199-4190TG[18]	NM_001319126.2:c.-199-4190TG[19]	NM_001319126.2:c.-199-4190TG[21]	NM_001319126.2:c.-199-4190TG[22]	NM_001319126.2:c.-199-4190TG[23]	NM_001319126.2:c.-199-4190TG[24]	NM_001319126.2:c.-199-4190TG[25]	NM_001319126.2:c.-199-4190TG[26]	NM_001319126.2:c.-199-4190TG[28]
ZNF431 transcript variant 4	NM_001319127.2:c.-305-4190=	NM_001319127.2:c.-305-4190TG[5]	NM_001319127.2:c.-305-4190TG[11]	NM_001319127.2:c.-305-4190TG[12]	NM_001319127.2:c.-305-4190TG[13]	NM_001319127.2:c.-305-4190TG[14]	NM_001319127.2:c.-305-4190TG[15]	NM_001319127.2:c.-305-4190TG[16]	NM_001319127.2:c.-305-4190TG[17]	NM_001319127.2:c.-305-4190TG[18]	NM_001319127.2:c.-305-4190TG[19]	NM_001319127.2:c.-305-4190TG[21]	NM_001319127.2:c.-305-4190TG[22]	NM_001319127.2:c.-305-4190TG[23]	NM_001319127.2:c.-305-4190TG[24]	NM_001319127.2:c.-305-4190TG[25]	NM_001319127.2:c.-305-4190TG[26]	NM_001319127.2:c.-305-4190TG[28]
ZNF431 transcript variant 2	NM_133473.2:c.97-4190=	NM_133473.2:c.97-4190TG[5]	NM_133473.2:c.97-4190TG[11]	NM_133473.2:c.97-4190TG[12]	NM_133473.2:c.97-4190TG[13]	NM_133473.2:c.97-4190TG[14]	NM_133473.2:c.97-4190TG[15]	NM_133473.2:c.97-4190TG[16]	NM_133473.2:c.97-4190TG[17]	NM_133473.2:c.97-4190TG[18]	NM_133473.2:c.97-4190TG[19]	NM_133473.2:c.97-4190TG[21]	NM_133473.2:c.97-4190TG[22]	NM_133473.2:c.97-4190TG[23]	NM_133473.2:c.97-4190TG[24]	NM_133473.2:c.97-4190TG[25]	NM_133473.2:c.97-4190TG[26]	NM_133473.2:c.97-4190TG[28]
ZNF431 transcript variant 2	NM_133473.4:c.97-4190=	NM_133473.4:c.97-4190TG[5]	NM_133473.4:c.97-4190TG[11]	NM_133473.4:c.97-4190TG[12]	NM_133473.4:c.97-4190TG[13]	NM_133473.4:c.97-4190TG[14]	NM_133473.4:c.97-4190TG[15]	NM_133473.4:c.97-4190TG[16]	NM_133473.4:c.97-4190TG[17]	NM_133473.4:c.97-4190TG[18]	NM_133473.4:c.97-4190TG[19]	NM_133473.4:c.97-4190TG[21]	NM_133473.4:c.97-4190TG[22]	NM_133473.4:c.97-4190TG[23]	NM_133473.4:c.97-4190TG[24]	NM_133473.4:c.97-4190TG[25]	NM_133473.4:c.97-4190TG[26]	NM_133473.4:c.97-4190TG[28]
ZNF431 transcript variant X1	XM_005259794.1:c.97-4190=	XM_005259794.1:c.97-4190TG[5]	XM_005259794.1:c.97-4190TG[11]	XM_005259794.1:c.97-4190TG[12]	XM_005259794.1:c.97-4190TG[13]	XM_005259794.1:c.97-4190TG[14]	XM_005259794.1:c.97-4190TG[15]	XM_005259794.1:c.97-4190TG[16]	XM_005259794.1:c.97-4190TG[17]	XM_005259794.1:c.97-4190TG[18]	XM_005259794.1:c.97-4190TG[19]	XM_005259794.1:c.97-4190TG[21]	XM_005259794.1:c.97-4190TG[22]	XM_005259794.1:c.97-4190TG[23]	XM_005259794.1:c.97-4190TG[24]	XM_005259794.1:c.97-4190TG[25]	XM_005259794.1:c.97-4190TG[26]	XM_005259794.1:c.97-4190TG[28]
ZNF431 transcript variant X2	XM_005259795.1:c.-202-4190=	XM_005259795.1:c.-202-4190TG[5]	XM_005259795.1:c.-202-4190TG[11]	XM_005259795.1:c.-202-4190TG[12]	XM_005259795.1:c.-202-4190TG[13]	XM_005259795.1:c.-202-4190TG[14]	XM_005259795.1:c.-202-4190TG[15]	XM_005259795.1:c.-202-4190TG[16]	XM_005259795.1:c.-202-4190TG[17]	XM_005259795.1:c.-202-4190TG[18]	XM_005259795.1:c.-202-4190TG[19]	XM_005259795.1:c.-202-4190TG[21]	XM_005259795.1:c.-202-4190TG[22]	XM_005259795.1:c.-202-4190TG[23]	XM_005259795.1:c.-202-4190TG[24]	XM_005259795.1:c.-202-4190TG[25]	XM_005259795.1:c.-202-4190TG[26]	XM_005259795.1:c.-202-4190TG[28]
ZNF431 transcript variant X4	XM_005259797.1:c.-199-4190=	XM_005259797.1:c.-199-4190TG[5]	XM_005259797.1:c.-199-4190TG[11]	XM_005259797.1:c.-199-4190TG[12]	XM_005259797.1:c.-199-4190TG[13]	XM_005259797.1:c.-199-4190TG[14]	XM_005259797.1:c.-199-4190TG[15]	XM_005259797.1:c.-199-4190TG[16]	XM_005259797.1:c.-199-4190TG[17]	XM_005259797.1:c.-199-4190TG[18]	XM_005259797.1:c.-199-4190TG[19]	XM_005259797.1:c.-199-4190TG[21]	XM_005259797.1:c.-199-4190TG[22]	XM_005259797.1:c.-199-4190TG[23]	XM_005259797.1:c.-199-4190TG[24]	XM_005259797.1:c.-199-4190TG[25]	XM_005259797.1:c.-199-4190TG[26]	XM_005259797.1:c.-199-4190TG[28]

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#.

47 SubSNP, 32 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss80512533	Oct 12, 2018 (152)
2	HUMANGENOME_JCVI	ss95724648	Mar 15, 2016 (147)
3	EVA_UK10K_TWINSUK	ss1709155863	Apr 01, 2015 (144)
4	EVA_UK10K_ALSPAC	ss1709155871	Apr 01, 2015 (144)
5	EVA_UK10K_ALSPAC	ss1710785463	Apr 01, 2015 (144)
6	EVA_UK10K_TWINSUK	ss1710785464	Apr 01, 2015 (144)
7	SWEGEN	ss3017246669	Nov 08, 2017 (151)
8	MCHAISSO	ss3063911226	Nov 08, 2017 (151)
9	MCHAISSO	ss3064758677	Nov 08, 2017 (151)
10	MCHAISSO	ss3065706373	Nov 08, 2017 (151)
11	EVA_DECODE	ss3702518681	Jul 13, 2019 (153)
12	EVA_DECODE	ss3702518682	Jul 13, 2019 (153)
13	EVA_DECODE	ss3702518683	Jul 13, 2019 (153)
14	GNOMAD	ss4329147360	Apr 26, 2021 (155)
15	GNOMAD	ss4329147361	Apr 26, 2021 (155)
16	GNOMAD	ss4329147362	Apr 26, 2021 (155)
17	GNOMAD	ss4329147363	Apr 26, 2021 (155)
18	GNOMAD	ss4329147364	Apr 26, 2021 (155)
19	GNOMAD	ss4329147365	Apr 26, 2021 (155)
20	GNOMAD	ss4329147366	Apr 26, 2021 (155)
21	GNOMAD	ss4329147373	Apr 26, 2021 (155)
22	GNOMAD	ss4329147374	Apr 26, 2021 (155)
23	GNOMAD	ss4329147375	Apr 26, 2021 (155)
24	GNOMAD	ss4329147376	Apr 26, 2021 (155)
25	GNOMAD	ss4329147377	Apr 26, 2021 (155)
26	GNOMAD	ss4329147378	Apr 26, 2021 (155)
27	GNOMAD	ss4329147379	Apr 26, 2021 (155)
28	GNOMAD	ss4329147380	Apr 26, 2021 (155)
29	TOPMED	ss5070720324	Apr 26, 2021 (155)
30	TOMMO_GENOMICS	ss5227159240	Apr 26, 2021 (155)
31	TOMMO_GENOMICS	ss5227159242	Apr 26, 2021 (155)
32	TOMMO_GENOMICS	ss5227159243	Apr 26, 2021 (155)
33	TOMMO_GENOMICS	ss5227159244	Apr 26, 2021 (155)
34	TOMMO_GENOMICS	ss5227159245	Apr 26, 2021 (155)
35	HUGCELL_USP	ss5499390353	Oct 16, 2022 (156)
36	HUGCELL_USP	ss5499390354	Oct 16, 2022 (156)
37	HUGCELL_USP	ss5499390356	Oct 16, 2022 (156)
38	HUGCELL_USP	ss5499390357	Oct 16, 2022 (156)
39	HUGCELL_USP	ss5499390358	Oct 16, 2022 (156)
40	TOMMO_GENOMICS	ss5785585072	Oct 16, 2022 (156)
41	TOMMO_GENOMICS	ss5785585073	Oct 16, 2022 (156)
42	TOMMO_GENOMICS	ss5785585075	Oct 16, 2022 (156)
43	TOMMO_GENOMICS	ss5785585076	Oct 16, 2022 (156)
44	TOMMO_GENOMICS	ss5785585077	Oct 16, 2022 (156)
45	EVA	ss5840375610	Oct 16, 2022 (156)
46	EVA	ss5840375611	Oct 16, 2022 (156)
47	EVA	ss5852237778	Oct 16, 2022 (156)
48	The Avon Longitudinal Study of Parents and Children	NC_000019.9 - 21344948	Oct 12, 2018 (152)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 536487726 (NC_000019.10:21162144::TG 2497/61686) Row 536487727 (NC_000019.10:21162144::TGTG 1188/61712) Row 536487728 (NC_000019.10:21162144::TGTGTG 526/61768)...	-	Apr 26, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 536487726 (NC_000019.10:21162144::TG 2497/61686) Row 536487727 (NC_000019.10:21162144::TGTG 1188/61712) Row 536487728 (NC_000019.10:21162144::TGTGTG 526/61768)...	-	Apr 26, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 536487726 (NC_000019.10:21162144::TG 2497/61686) Row 536487727 (NC_000019.10:21162144::TGTG 1188/61712) Row 536487728 (NC_000019.10:21162144::TGTGTG 526/61768)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 536487726 (NC_000019.10:21162144::TG 2497/61686) Row 536487727 (NC_000019.10:21162144::TGTG 1188/61712) Row 536487728 (NC_000019.10:21162144::TGTGTG 526/61768)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 536487726 (NC_000019.10:21162144::TG 2497/61686) Row 536487727 (NC_000019.10:21162144::TGTG 1188/61712) Row 536487728 (NC_000019.10:21162144::TGTGTG 526/61768)...	-	Apr 26, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 536487726 (NC_000019.10:21162144::TG 2497/61686) Row 536487727 (NC_000019.10:21162144::TGTG 1188/61712) Row 536487728 (NC_000019.10:21162144::TGTGTG 526/61768)...	-	Apr 26, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 536487726 (NC_000019.10:21162144::TG 2497/61686) Row 536487727 (NC_000019.10:21162144::TGTG 1188/61712) Row 536487728 (NC_000019.10:21162144::TGTGTG 526/61768)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 536487726 (NC_000019.10:21162144::TG 2497/61686) Row 536487727 (NC_000019.10:21162144::TGTG 1188/61712) Row 536487728 (NC_000019.10:21162144::TGTGTG 526/61768)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 536487726 (NC_000019.10:21162144::TG 2497/61686) Row 536487727 (NC_000019.10:21162144::TGTG 1188/61712) Row 536487728 (NC_000019.10:21162144::TGTGTG 526/61768)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 536487726 (NC_000019.10:21162144::TG 2497/61686) Row 536487727 (NC_000019.10:21162144::TGTG 1188/61712) Row 536487728 (NC_000019.10:21162144::TGTGTG 526/61768)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 536487726 (NC_000019.10:21162144::TG 2497/61686) Row 536487727 (NC_000019.10:21162144::TGTG 1188/61712) Row 536487728 (NC_000019.10:21162144::TGTGTG 526/61768)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 536487726 (NC_000019.10:21162144::TG 2497/61686) Row 536487727 (NC_000019.10:21162144::TGTG 1188/61712) Row 536487728 (NC_000019.10:21162144::TGTGTG 526/61768)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 536487726 (NC_000019.10:21162144::TG 2497/61686) Row 536487727 (NC_000019.10:21162144::TGTG 1188/61712) Row 536487728 (NC_000019.10:21162144::TGTGTG 526/61768)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 536487726 (NC_000019.10:21162144::TG 2497/61686) Row 536487727 (NC_000019.10:21162144::TGTG 1188/61712) Row 536487728 (NC_000019.10:21162144::TGTGTG 526/61768)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 536487726 (NC_000019.10:21162144::TG 2497/61686) Row 536487727 (NC_000019.10:21162144::TGTG 1188/61712) Row 536487728 (NC_000019.10:21162144::TGTGTG 526/61768)...	-	Apr 26, 2021 (155)
64	8.3KJPN Submission ignored due to conflicting rows: Row 85128547 (NC_000019.9:21344947:TG: 785/10616) Row 85128549 (NC_000019.9:21344947:TGTG: 2740/10616) Row 85128550 (NC_000019.9:21344947::TG 13/10616)...	-	Apr 26, 2021 (155)
65	8.3KJPN Submission ignored due to conflicting rows: Row 85128547 (NC_000019.9:21344947:TG: 785/10616) Row 85128549 (NC_000019.9:21344947:TGTG: 2740/10616) Row 85128550 (NC_000019.9:21344947::TG 13/10616)...	-	Apr 26, 2021 (155)
66	8.3KJPN Submission ignored due to conflicting rows: Row 85128547 (NC_000019.9:21344947:TG: 785/10616) Row 85128549 (NC_000019.9:21344947:TGTG: 2740/10616) Row 85128550 (NC_000019.9:21344947::TG 13/10616)...	-	Apr 26, 2021 (155)
67	8.3KJPN Submission ignored due to conflicting rows: Row 85128547 (NC_000019.9:21344947:TG: 785/10616) Row 85128549 (NC_000019.9:21344947:TGTG: 2740/10616) Row 85128550 (NC_000019.9:21344947::TG 13/10616)...	-	Apr 26, 2021 (155)
68	8.3KJPN Submission ignored due to conflicting rows: Row 85128547 (NC_000019.9:21344947:TG: 785/10616) Row 85128549 (NC_000019.9:21344947:TGTG: 2740/10616) Row 85128550 (NC_000019.9:21344947::TG 13/10616)...	-	Apr 26, 2021 (155)
69	14KJPN Submission ignored due to conflicting rows: Row 119422176 (NC_000019.10:21162144:TGTG: 4631/28242) Row 119422177 (NC_000019.10:21162144:TG: 1302/28242) Row 119422179 (NC_000019.10:21162144::TG 18/28242)...	-	Oct 16, 2022 (156)
70	14KJPN Submission ignored due to conflicting rows: Row 119422176 (NC_000019.10:21162144:TGTG: 4631/28242) Row 119422177 (NC_000019.10:21162144:TG: 1302/28242) Row 119422179 (NC_000019.10:21162144::TG 18/28242)...	-	Oct 16, 2022 (156)
71	14KJPN Submission ignored due to conflicting rows: Row 119422176 (NC_000019.10:21162144:TGTG: 4631/28242) Row 119422177 (NC_000019.10:21162144:TG: 1302/28242) Row 119422179 (NC_000019.10:21162144::TG 18/28242)...	-	Oct 16, 2022 (156)
72	14KJPN Submission ignored due to conflicting rows: Row 119422176 (NC_000019.10:21162144:TGTG: 4631/28242) Row 119422177 (NC_000019.10:21162144:TG: 1302/28242) Row 119422179 (NC_000019.10:21162144::TG 18/28242)...	-	Oct 16, 2022 (156)
73	14KJPN Submission ignored due to conflicting rows: Row 119422176 (NC_000019.10:21162144:TGTG: 4631/28242) Row 119422177 (NC_000019.10:21162144:TG: 1302/28242) Row 119422179 (NC_000019.10:21162144::TG 18/28242)...	-	Oct 16, 2022 (156)
74	TopMed	NC_000019.10 - 21162145	Apr 26, 2021 (155)
75	UK 10K study - Twins Submission ignored due to conflicting rows: Row 42135800 (NC_000019.9:21344949:TG: 1183/3708) Row 42135801 (NC_000019.9:21344947:TGTG: 306/3708)	-	Apr 27, 2020 (154)
76	UK 10K study - Twins	-	Oct 12, 2018 (152)
77	A Vietnamese Genetic Variation Database Submission ignored due to conflicting rows: Row 9310449 (NC_000019.9:21344947:TGTG: 22/119) Row 9310450 (NC_000019.9:21344947:TG: 8/105)	-	Jul 13, 2019 (153)
78	A Vietnamese Genetic Variation Database Submission ignored due to conflicting rows: Row 9310449 (NC_000019.9:21344947:TGTG: 22/119) Row 9310450 (NC_000019.9:21344947:TG: 8/105)	-	Jul 13, 2019 (153)
79	ALFA	NC_000019.10 - 21162145	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
286265988, ss5070720324	NC_000019.10:21162144:TGTGTGTGTGTG… NC_000019.10:21162144:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:	NC_000019.10:21162144:TGTGTGTGTGTG… NC_000019.10:21162144:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGT	(self)
4313494393	NC_000019.10:21162144:TGTGTGTGTGTG… NC_000019.10:21162144:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGT	NC_000019.10:21162144:TGTGTGTGTGTG… NC_000019.10:21162144:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGT	(self)
4313494393	NC_000019.10:21162144:TGTGTGTGTGTG… NC_000019.10:21162144:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGT	NC_000019.10:21162144:TGTGTGTGTGTG… NC_000019.10:21162144:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4329147380	NC_000019.10:21162144:TGTGTGTGTGTG… NC_000019.10:21162144:TGTGTGTGTGTGTGTG:	NC_000019.10:21162144:TGTGTGTGTGTG… NC_000019.10:21162144:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGT	(self)
4313494393	NC_000019.10:21162144:TGTGTGTGTGTG… NC_000019.10:21162144:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGT	NC_000019.10:21162144:TGTGTGTGTGTG… NC_000019.10:21162144:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4329147379	NC_000019.10:21162144:TGTGTGTGTGTG… NC_000019.10:21162144:TGTGTGTGTGTGTG:	NC_000019.10:21162144:TGTGTGTGTGTG… NC_000019.10:21162144:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
4313494393	NC_000019.10:21162144:TGTGTGTGTGTG… NC_000019.10:21162144:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000019.10:21162144:TGTGTGTGTGTG… NC_000019.10:21162144:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3017246669	NC_000019.9:21344947:TGTGTGTGTGTG:	NC_000019.10:21162144:TGTGTGTGTGTG… NC_000019.10:21162144:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4329147378	NC_000019.10:21162144:TGTGTGTGTGTG:	NC_000019.10:21162144:TGTGTGTGTGTG… NC_000019.10:21162144:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
4313494393	NC_000019.10:21162144:TGTGTGTGTGTG… NC_000019.10:21162144:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000019.10:21162144:TGTGTGTGTGTG… NC_000019.10:21162144:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4329147377	NC_000019.10:21162144:TGTGTGTGTG:	NC_000019.10:21162144:TGTGTGTGTGTG… NC_000019.10:21162144:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
4313494393	NC_000019.10:21162144:TGTGTGTGTGTG… NC_000019.10:21162144:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000019.10:21162144:TGTGTGTGTGTG… NC_000019.10:21162144:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss5227159245	NC_000019.9:21344947:TGTGTGTG:	NC_000019.10:21162144:TGTGTGTGTGTG… NC_000019.10:21162144:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4329147376, ss5785585077	NC_000019.10:21162144:TGTGTGTG:	NC_000019.10:21162144:TGTGTGTGTGTG… NC_000019.10:21162144:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
4313494393	NC_000019.10:21162144:TGTGTGTGTGTG… NC_000019.10:21162144:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000019.10:21162144:TGTGTGTGTGTG… NC_000019.10:21162144:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss5227159244	NC_000019.9:21344947:TGTGTG:	NC_000019.10:21162144:TGTGTGTGTGTG… NC_000019.10:21162144:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3702518681, ss4329147375, ss5499390356, ss5785585076	NC_000019.10:21162144:TGTGTG:	NC_000019.10:21162144:TGTGTGTGTGTG… NC_000019.10:21162144:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
4313494393	NC_000019.10:21162144:TGTGTGTGTGTG… NC_000019.10:21162144:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000019.10:21162144:TGTGTGTGTGTG… NC_000019.10:21162144:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
42135801, ss1709155863, ss1709155871, ss5227159242, ss5840375611	NC_000019.9:21344947:TGTG:	NC_000019.10:21162144:TGTGTGTGTGTG… NC_000019.10:21162144:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3063911226, ss3064758677, ss3065706373, ss4329147374, ss5499390353, ss5785585072, ss5852237778	NC_000019.10:21162144:TGTG:	NC_000019.10:21162144:TGTGTGTGTGTG… NC_000019.10:21162144:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
4313494393	NC_000019.10:21162144:TGTGTGTGTGTG… NC_000019.10:21162144:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000019.10:21162144:TGTGTGTGTGTG… NC_000019.10:21162144:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3702518682	NC_000019.10:21162146:TGTG:	NC_000019.10:21162144:TGTGTGTGTGTG… NC_000019.10:21162144:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss5227159240, ss5840375610	NC_000019.9:21344947:TG:	NC_000019.10:21162144:TGTGTGTGTGTG… NC_000019.10:21162144:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss1710785463, ss1710785464	NC_000019.9:21344949:TG:	NC_000019.10:21162144:TGTGTGTGTGTG… NC_000019.10:21162144:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4329147373, ss5499390354, ss5785585073	NC_000019.10:21162144:TG:	NC_000019.10:21162144:TGTGTGTGTGTG… NC_000019.10:21162144:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
4313494393	NC_000019.10:21162144:TGTGTGTGTGTG… NC_000019.10:21162144:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000019.10:21162144:TGTGTGTGTGTG… NC_000019.10:21162144:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3702518683	NC_000019.10:21162148:TG:	NC_000019.10:21162144:TGTGTGTGTGTG… NC_000019.10:21162144:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss5227159243	NC_000019.9:21344947::TG	NC_000019.10:21162144:TGTGTGTGTGTG… NC_000019.10:21162144:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4329147360, ss5499390357, ss5785585075	NC_000019.10:21162144::TG	NC_000019.10:21162144:TGTGTGTGTGTG… NC_000019.10:21162144:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
4313494393	NC_000019.10:21162144:TGTGTGTGTGTG… NC_000019.10:21162144:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000019.10:21162144:TGTGTGTGTGTG… NC_000019.10:21162144:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss95724648	NT_011295.11:12607752:G:GTG	NC_000019.10:21162144:TGTGTGTGTGTG… NC_000019.10:21162144:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss80512533	NT_011295.11:12607790::GT	NC_000019.10:21162144:TGTGTGTGTGTG… NC_000019.10:21162144:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4329147361, ss5499390358	NC_000019.10:21162144::TGTG	NC_000019.10:21162144:TGTGTGTGTGTG… NC_000019.10:21162144:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
4313494393	NC_000019.10:21162144:TGTGTGTGTGTG… NC_000019.10:21162144:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000019.10:21162144:TGTGTGTGTGTG… NC_000019.10:21162144:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4329147362	NC_000019.10:21162144::TGTGTG	NC_000019.10:21162144:TGTGTGTGTGTG… NC_000019.10:21162144:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
4313494393	NC_000019.10:21162144:TGTGTGTGTGTG… NC_000019.10:21162144:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000019.10:21162144:TGTGTGTGTGTG… NC_000019.10:21162144:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4329147363	NC_000019.10:21162144::TGTGTGTG	NC_000019.10:21162144:TGTGTGTGTGTG… NC_000019.10:21162144:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
4313494393	NC_000019.10:21162144:TGTGTGTGTGTG… NC_000019.10:21162144:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000019.10:21162144:TGTGTGTGTGTG… NC_000019.10:21162144:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4329147364	NC_000019.10:21162144::TGTGTGTGTG	NC_000019.10:21162144:TGTGTGTGTGTG… NC_000019.10:21162144:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
4313494393	NC_000019.10:21162144:TGTGTGTGTGTG… NC_000019.10:21162144:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000019.10:21162144:TGTGTGTGTGTG… NC_000019.10:21162144:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4329147365	NC_000019.10:21162144::TGTGTGTGTGTG	NC_000019.10:21162144:TGTGTGTGTGTG… NC_000019.10:21162144:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
4313494393	NC_000019.10:21162144:TGTGTGTGTGTG… NC_000019.10:21162144:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000019.10:21162144:TGTGTGTGTGTG… NC_000019.10:21162144:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4329147366	NC_000019.10:21162144::TGTGTGTGTGT… NC_000019.10:21162144::TGTGTGTGTGTGTGTG	NC_000019.10:21162144:TGTGTGTGTGTG… NC_000019.10:21162144:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3290059237	NC_000019.10:21162144:TGTGTGTGTGTG… NC_000019.10:21162144:TGTGTGTGTGTGTGTGTG:	NC_000019.10:21162144:TGTGTGTGTGTG… NC_000019.10:21162144:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGT

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

No publications for rs749424799

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.
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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs749424799