Name: rs71820531
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.

rs71820531

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chrX:119471777-119471804 (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)₁₉ / del(T)₁₈ / del(T)₁₇ / d…
del(T)₁₉ / 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 / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₅ / dup(T)₆ / dup(T)₇ / dup(T)₈ / dup(T)₉ / dup(T)₁₀
Variation Type: Indel Insertion and Deletion
Frequency: dupTTT=0.1019 (817/8014, ALFA)
(T)₂₈=0.2948 (1113/3775, 1000G)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: SLC25A5 : 500B Downstream Variant
Publications: 0 citations
Genomic View: See rs on genome

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

Release Version: 20231103111315

Population	Group	Sample Size	Ref Allele	Alt Allele	Ref HMOZ	Alt HMOZ	HTRZ	HWEP
Total	Global	8014	TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.8223	TTTTTTTTT=0.0000, TTTTTTTTTT=0.0389, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, 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, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0198, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0080, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.1019, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0090, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.883629	0.094393	0.021978	32
European	Sub	7074	TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.7990	TTTTTTTTT=0.0000, TTTTTTTTTT=0.0438, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, 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, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0225, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0090, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.1155, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0102, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.865909	0.108766	0.025325	32
African	Sub	514	TTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, 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, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	16	TTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, 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, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	498	TTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, 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, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	38	TTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, 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, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	34	TTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, 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, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	4	TTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTT=0.0, TTTTTTTTTT=0.0, TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	40	TTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, 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, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	162	TTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, 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, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	22	TTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, 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, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	164	TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.988	TTTTTTTTT=0.000, TTTTTTTTTT=0.012, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, 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, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A

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

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	8014	(T)₂₈=0.8223	del(T)₁₉=0.0000, del(T)₁₈=0.0389, 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, delTTT=0.0000, delTT=0.0198, delT=0.0000, dupT=0.0080, dupTT=0.0000, dupTTT=0.1019, dup(T)₄=0.0090, dup(T)₅=0.0000, dup(T)₆=0.0000
Allele Frequency Aggregator	European	Sub	7074	(T)₂₈=0.7990	del(T)₁₉=0.0000, del(T)₁₈=0.0438, 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, delTTT=0.0000, delTT=0.0225, delT=0.0000, dupT=0.0090, dupTT=0.0000, dupTTT=0.1155, dup(T)₄=0.0102, dup(T)₅=0.0000, dup(T)₆=0.0000
Allele Frequency Aggregator	African	Sub	514	(T)₂₈=1.000	del(T)₁₉=0.000, 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, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₅=0.000, dup(T)₆=0.000
Allele Frequency Aggregator	Other	Sub	164	(T)₂₈=0.988	del(T)₁₉=0.000, del(T)₁₈=0.012, 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, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₅=0.000, dup(T)₆=0.000
Allele Frequency Aggregator	Latin American 2	Sub	162	(T)₂₈=1.000	del(T)₁₉=0.000, 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, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₅=0.000, dup(T)₆=0.000
Allele Frequency Aggregator	Latin American 1	Sub	40	(T)₂₈=1.00	del(T)₁₉=0.00, 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, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₅=0.00, dup(T)₆=0.00
Allele Frequency Aggregator	Asian	Sub	38	(T)₂₈=1.00	del(T)₁₉=0.00, 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, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₅=0.00, dup(T)₆=0.00
Allele Frequency Aggregator	South Asian	Sub	22	(T)₂₈=1.00	del(T)₁₉=0.00, 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, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₅=0.00, dup(T)₆=0.00
1000Genomes	Global	Study-wide	3775	(T)₂₈=0.2948	del(T)₁₈=0.7052
1000Genomes	African	Sub	1003	(T)₂₈=0.2552	del(T)₁₈=0.7448
1000Genomes	Europe	Sub	766	(T)₂₈=0.320	del(T)₁₈=0.680
1000Genomes	East Asian	Sub	764	(T)₂₈=0.351	del(T)₁₈=0.649
1000Genomes	South Asian	Sub	718	(T)₂₈=0.280	del(T)₁₈=0.720
1000Genomes	American	Sub	524	(T)₂₈=0.273	del(T)₁₈=0.727

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 X	NC_000023.11:g.119471786_119471804del
GRCh38.p14 chr X	NC_000023.11:g.119471787_119471804del
GRCh38.p14 chr X	NC_000023.11:g.119471788_119471804del
GRCh38.p14 chr X	NC_000023.11:g.119471789_119471804del
GRCh38.p14 chr X	NC_000023.11:g.119471790_119471804del
GRCh38.p14 chr X	NC_000023.11:g.119471791_119471804del
GRCh38.p14 chr X	NC_000023.11:g.119471792_119471804del
GRCh38.p14 chr X	NC_000023.11:g.119471793_119471804del
GRCh38.p14 chr X	NC_000023.11:g.119471794_119471804del
GRCh38.p14 chr X	NC_000023.11:g.119471795_119471804del
GRCh38.p14 chr X	NC_000023.11:g.119471796_119471804del
GRCh38.p14 chr X	NC_000023.11:g.119471797_119471804del
GRCh38.p14 chr X	NC_000023.11:g.119471798_119471804del
GRCh38.p14 chr X	NC_000023.11:g.119471799_119471804del
GRCh38.p14 chr X	NC_000023.11:g.119471800_119471804del
GRCh38.p14 chr X	NC_000023.11:g.119471802_119471804del
GRCh38.p14 chr X	NC_000023.11:g.119471803_119471804del
GRCh38.p14 chr X	NC_000023.11:g.119471804del
GRCh38.p14 chr X	NC_000023.11:g.119471804dup
GRCh38.p14 chr X	NC_000023.11:g.119471803_119471804dup
GRCh38.p14 chr X	NC_000023.11:g.119471802_119471804dup
GRCh38.p14 chr X	NC_000023.11:g.119471801_119471804dup
GRCh38.p14 chr X	NC_000023.11:g.119471800_119471804dup
GRCh38.p14 chr X	NC_000023.11:g.119471799_119471804dup
GRCh38.p14 chr X	NC_000023.11:g.119471798_119471804dup
GRCh38.p14 chr X	NC_000023.11:g.119471797_119471804dup
GRCh38.p14 chr X	NC_000023.11:g.119471796_119471804dup
GRCh38.p14 chr X	NC_000023.11:g.119471795_119471804dup
GRCh37.p13 chr X	NC_000023.10:g.118605749_118605767del
GRCh37.p13 chr X	NC_000023.10:g.118605750_118605767del
GRCh37.p13 chr X	NC_000023.10:g.118605751_118605767del
GRCh37.p13 chr X	NC_000023.10:g.118605752_118605767del
GRCh37.p13 chr X	NC_000023.10:g.118605753_118605767del
GRCh37.p13 chr X	NC_000023.10:g.118605754_118605767del
GRCh37.p13 chr X	NC_000023.10:g.118605755_118605767del
GRCh37.p13 chr X	NC_000023.10:g.118605756_118605767del
GRCh37.p13 chr X	NC_000023.10:g.118605757_118605767del
GRCh37.p13 chr X	NC_000023.10:g.118605758_118605767del
GRCh37.p13 chr X	NC_000023.10:g.118605759_118605767del
GRCh37.p13 chr X	NC_000023.10:g.118605760_118605767del
GRCh37.p13 chr X	NC_000023.10:g.118605761_118605767del
GRCh37.p13 chr X	NC_000023.10:g.118605762_118605767del
GRCh37.p13 chr X	NC_000023.10:g.118605763_118605767del
GRCh37.p13 chr X	NC_000023.10:g.118605765_118605767del
GRCh37.p13 chr X	NC_000023.10:g.118605766_118605767del
GRCh37.p13 chr X	NC_000023.10:g.118605767del
GRCh37.p13 chr X	NC_000023.10:g.118605767dup
GRCh37.p13 chr X	NC_000023.10:g.118605766_118605767dup
GRCh37.p13 chr X	NC_000023.10:g.118605765_118605767dup
GRCh37.p13 chr X	NC_000023.10:g.118605764_118605767dup
GRCh37.p13 chr X	NC_000023.10:g.118605763_118605767dup
GRCh37.p13 chr X	NC_000023.10:g.118605762_118605767dup
GRCh37.p13 chr X	NC_000023.10:g.118605761_118605767dup
GRCh37.p13 chr X	NC_000023.10:g.118605760_118605767dup
GRCh37.p13 chr X	NC_000023.10:g.118605759_118605767dup
GRCh37.p13 chr X	NC_000023.10:g.118605758_118605767dup
SLC25A5 RefSeqGene	NG_013262.1:g.8387_8405del
SLC25A5 RefSeqGene	NG_013262.1:g.8388_8405del
SLC25A5 RefSeqGene	NG_013262.1:g.8389_8405del
SLC25A5 RefSeqGene	NG_013262.1:g.8390_8405del
SLC25A5 RefSeqGene	NG_013262.1:g.8391_8405del
SLC25A5 RefSeqGene	NG_013262.1:g.8392_8405del
SLC25A5 RefSeqGene	NG_013262.1:g.8393_8405del
SLC25A5 RefSeqGene	NG_013262.1:g.8394_8405del
SLC25A5 RefSeqGene	NG_013262.1:g.8395_8405del
SLC25A5 RefSeqGene	NG_013262.1:g.8396_8405del
SLC25A5 RefSeqGene	NG_013262.1:g.8397_8405del
SLC25A5 RefSeqGene	NG_013262.1:g.8398_8405del
SLC25A5 RefSeqGene	NG_013262.1:g.8399_8405del
SLC25A5 RefSeqGene	NG_013262.1:g.8400_8405del
SLC25A5 RefSeqGene	NG_013262.1:g.8401_8405del
SLC25A5 RefSeqGene	NG_013262.1:g.8403_8405del
SLC25A5 RefSeqGene	NG_013262.1:g.8404_8405del
SLC25A5 RefSeqGene	NG_013262.1:g.8405del
SLC25A5 RefSeqGene	NG_013262.1:g.8405dup
SLC25A5 RefSeqGene	NG_013262.1:g.8404_8405dup
SLC25A5 RefSeqGene	NG_013262.1:g.8403_8405dup
SLC25A5 RefSeqGene	NG_013262.1:g.8402_8405dup
SLC25A5 RefSeqGene	NG_013262.1:g.8401_8405dup
SLC25A5 RefSeqGene	NG_013262.1:g.8400_8405dup
SLC25A5 RefSeqGene	NG_013262.1:g.8399_8405dup
SLC25A5 RefSeqGene	NG_013262.1:g.8398_8405dup
SLC25A5 RefSeqGene	NG_013262.1:g.8397_8405dup
SLC25A5 RefSeqGene	NG_013262.1:g.8396_8405dup

Gene: SLC25A5, solute carrier family 25 member 5 (plus strand) : 500B Downstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
SLC25A5 transcript	NM_001152.5:c.	N/A	Downstream Transcript Variant

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

Not Reported in ClinVar

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

Placement	(T)₂₈=	del(T)₁₉	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	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₅	dup(T)₆	dup(T)₇	dup(T)₈	dup(T)₉	dup(T)₁₀
GRCh38.p14 chr X	NC_000023.11:g.119471777_119471804=	NC_000023.11:g.119471786_119471804del	NC_000023.11:g.119471787_119471804del	NC_000023.11:g.119471788_119471804del	NC_000023.11:g.119471789_119471804del	NC_000023.11:g.119471790_119471804del	NC_000023.11:g.119471791_119471804del	NC_000023.11:g.119471792_119471804del	NC_000023.11:g.119471793_119471804del	NC_000023.11:g.119471794_119471804del	NC_000023.11:g.119471795_119471804del	NC_000023.11:g.119471796_119471804del	NC_000023.11:g.119471797_119471804del	NC_000023.11:g.119471798_119471804del	NC_000023.11:g.119471799_119471804del	NC_000023.11:g.119471800_119471804del	NC_000023.11:g.119471802_119471804del	NC_000023.11:g.119471803_119471804del	NC_000023.11:g.119471804del	NC_000023.11:g.119471804dup	NC_000023.11:g.119471803_119471804dup	NC_000023.11:g.119471802_119471804dup	NC_000023.11:g.119471801_119471804dup	NC_000023.11:g.119471800_119471804dup	NC_000023.11:g.119471799_119471804dup	NC_000023.11:g.119471798_119471804dup	NC_000023.11:g.119471797_119471804dup	NC_000023.11:g.119471796_119471804dup	NC_000023.11:g.119471795_119471804dup
GRCh37.p13 chr X	NC_000023.10:g.118605740_118605767=	NC_000023.10:g.118605749_118605767del	NC_000023.10:g.118605750_118605767del	NC_000023.10:g.118605751_118605767del	NC_000023.10:g.118605752_118605767del	NC_000023.10:g.118605753_118605767del	NC_000023.10:g.118605754_118605767del	NC_000023.10:g.118605755_118605767del	NC_000023.10:g.118605756_118605767del	NC_000023.10:g.118605757_118605767del	NC_000023.10:g.118605758_118605767del	NC_000023.10:g.118605759_118605767del	NC_000023.10:g.118605760_118605767del	NC_000023.10:g.118605761_118605767del	NC_000023.10:g.118605762_118605767del	NC_000023.10:g.118605763_118605767del	NC_000023.10:g.118605765_118605767del	NC_000023.10:g.118605766_118605767del	NC_000023.10:g.118605767del	NC_000023.10:g.118605767dup	NC_000023.10:g.118605766_118605767dup	NC_000023.10:g.118605765_118605767dup	NC_000023.10:g.118605764_118605767dup	NC_000023.10:g.118605763_118605767dup	NC_000023.10:g.118605762_118605767dup	NC_000023.10:g.118605761_118605767dup	NC_000023.10:g.118605760_118605767dup	NC_000023.10:g.118605759_118605767dup	NC_000023.10:g.118605758_118605767dup
SLC25A5 RefSeqGene	NG_013262.1:g.8378_8405=	NG_013262.1:g.8387_8405del	NG_013262.1:g.8388_8405del	NG_013262.1:g.8389_8405del	NG_013262.1:g.8390_8405del	NG_013262.1:g.8391_8405del	NG_013262.1:g.8392_8405del	NG_013262.1:g.8393_8405del	NG_013262.1:g.8394_8405del	NG_013262.1:g.8395_8405del	NG_013262.1:g.8396_8405del	NG_013262.1:g.8397_8405del	NG_013262.1:g.8398_8405del	NG_013262.1:g.8399_8405del	NG_013262.1:g.8400_8405del	NG_013262.1:g.8401_8405del	NG_013262.1:g.8403_8405del	NG_013262.1:g.8404_8405del	NG_013262.1:g.8405del	NG_013262.1:g.8405dup	NG_013262.1:g.8404_8405dup	NG_013262.1:g.8403_8405dup	NG_013262.1:g.8402_8405dup	NG_013262.1:g.8401_8405dup	NG_013262.1:g.8400_8405dup	NG_013262.1:g.8399_8405dup	NG_013262.1:g.8398_8405dup	NG_013262.1:g.8397_8405dup	NG_013262.1:g.8396_8405dup

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#.

59 SubSNP, 45 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	TSC-CSHL	ss4309916	Mar 15, 2016 (147)
2	BCMHGSC_JDW	ss103794487	Dec 01, 2009 (131)
3	BUSHMAN	ss194066978	Mar 15, 2016 (147)
4	PJP	ss295462438	May 09, 2011 (135)
5	1000GENOMES	ss1555932653	Apr 01, 2015 (144)
6	EVA_UK10K_ALSPAC	ss1709838577	Apr 01, 2015 (144)
7	EVA_UK10K_TWINSUK	ss1709838807	Apr 01, 2015 (144)
8	EVA_UK10K_TWINSUK	ss1710874701	Apr 01, 2015 (144)
9	EVA_UK10K_ALSPAC	ss1710874702	Apr 01, 2015 (144)
10	SWEGEN	ss3020535968	Nov 08, 2017 (151)
11	MCHAISSO	ss3066305925	Nov 08, 2017 (151)
12	KHV_HUMAN_GENOMES	ss3823337731	Jul 14, 2019 (153)
13	EVA	ss3836293770	Apr 27, 2020 (154)
14	GNOMAD	ss4377808668	Apr 26, 2021 (155)
15	GNOMAD	ss4377808669	Apr 26, 2021 (155)
16	GNOMAD	ss4377808670	Apr 26, 2021 (155)
17	GNOMAD	ss4377808671	Apr 26, 2021 (155)
18	GNOMAD	ss4377808672	Apr 26, 2021 (155)
19	GNOMAD	ss4377808673	Apr 26, 2021 (155)
20	GNOMAD	ss4377808674	Apr 26, 2021 (155)
21	GNOMAD	ss4377808675	Apr 26, 2021 (155)
22	GNOMAD	ss4377808676	Apr 26, 2021 (155)
23	GNOMAD	ss4377808677	Apr 26, 2021 (155)
24	GNOMAD	ss4377808679	Apr 26, 2021 (155)
25	GNOMAD	ss4377808680	Apr 26, 2021 (155)
26	GNOMAD	ss4377808681	Apr 26, 2021 (155)
27	GNOMAD	ss4377808682	Apr 26, 2021 (155)
28	GNOMAD	ss4377808683	Apr 26, 2021 (155)
29	GNOMAD	ss4377808684	Apr 26, 2021 (155)
30	GNOMAD	ss4377808685	Apr 26, 2021 (155)
31	GNOMAD	ss4377808686	Apr 26, 2021 (155)
32	GNOMAD	ss4377808687	Apr 26, 2021 (155)
33	GNOMAD	ss4377808688	Apr 26, 2021 (155)
34	GNOMAD	ss4377808689	Apr 26, 2021 (155)
35	GNOMAD	ss4377808690	Apr 26, 2021 (155)
36	TOPMED	ss5135511438	Apr 26, 2021 (155)
37	TOPMED	ss5135511439	Apr 26, 2021 (155)
38	TOPMED	ss5135511440	Apr 26, 2021 (155)
39	TOPMED	ss5135511441	Apr 26, 2021 (155)
40	TOMMO_GENOMICS	ss5236041297	Apr 26, 2021 (155)
41	TOMMO_GENOMICS	ss5236041298	Apr 26, 2021 (155)
42	TOMMO_GENOMICS	ss5236041299	Apr 26, 2021 (155)
43	TOMMO_GENOMICS	ss5236041300	Apr 26, 2021 (155)
44	TOMMO_GENOMICS	ss5236041301	Apr 26, 2021 (155)
45	TOMMO_GENOMICS	ss5236041302	Apr 26, 2021 (155)
46	1000G_HIGH_COVERAGE	ss5313743565	Oct 17, 2022 (156)
47	1000G_HIGH_COVERAGE	ss5313743566	Oct 17, 2022 (156)
48	1000G_HIGH_COVERAGE	ss5313743567	Oct 17, 2022 (156)
49	1000G_HIGH_COVERAGE	ss5313743568	Oct 17, 2022 (156)
50	HUGCELL_USP	ss5505175436	Oct 17, 2022 (156)
51	HUGCELL_USP	ss5505175437	Oct 17, 2022 (156)
52	HUGCELL_USP	ss5505175438	Oct 17, 2022 (156)
53	TOMMO_GENOMICS	ss5798349738	Oct 17, 2022 (156)
54	TOMMO_GENOMICS	ss5798349739	Oct 17, 2022 (156)
55	TOMMO_GENOMICS	ss5798349740	Oct 17, 2022 (156)
56	TOMMO_GENOMICS	ss5798349741	Oct 17, 2022 (156)
57	TOMMO_GENOMICS	ss5798349742	Oct 17, 2022 (156)
58	TOMMO_GENOMICS	ss5798349743	Oct 17, 2022 (156)
59	EVA	ss5857182083	Oct 17, 2022 (156)
60	1000Genomes	NC_000023.10 - 118605740	Oct 12, 2018 (152)
61	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 46217794 (NC_000023.10:118605739:TTTTTTTTTTTTTTTTTT: 282/2889) Row 46217795 (NC_000023.10:118605739::TTT 2607/2889)	-	Oct 12, 2018 (152)
62	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 46217794 (NC_000023.10:118605739:TTTTTTTTTTTTTTTTTT: 282/2889) Row 46217795 (NC_000023.10:118605739::TTT 2607/2889)	-	Oct 12, 2018 (152)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 589992297 (NC_000023.11:119471776::T 3827/57605) Row 589992298 (NC_000023.11:119471776::TT 466/57959) Row 589992299 (NC_000023.11:119471776::TTT 19019/57539)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 589992297 (NC_000023.11:119471776::T 3827/57605) Row 589992298 (NC_000023.11:119471776::TT 466/57959) Row 589992299 (NC_000023.11:119471776::TTT 19019/57539)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 589992297 (NC_000023.11:119471776::T 3827/57605) Row 589992298 (NC_000023.11:119471776::TT 466/57959) Row 589992299 (NC_000023.11:119471776::TTT 19019/57539)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 589992297 (NC_000023.11:119471776::T 3827/57605) Row 589992298 (NC_000023.11:119471776::TT 466/57959) Row 589992299 (NC_000023.11:119471776::TTT 19019/57539)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 589992297 (NC_000023.11:119471776::T 3827/57605) Row 589992298 (NC_000023.11:119471776::TT 466/57959) Row 589992299 (NC_000023.11:119471776::TTT 19019/57539)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 589992297 (NC_000023.11:119471776::T 3827/57605) Row 589992298 (NC_000023.11:119471776::TT 466/57959) Row 589992299 (NC_000023.11:119471776::TTT 19019/57539)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 589992297 (NC_000023.11:119471776::T 3827/57605) Row 589992298 (NC_000023.11:119471776::TT 466/57959) Row 589992299 (NC_000023.11:119471776::TTT 19019/57539)...	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 589992297 (NC_000023.11:119471776::T 3827/57605) Row 589992298 (NC_000023.11:119471776::TT 466/57959) Row 589992299 (NC_000023.11:119471776::TTT 19019/57539)...	-	Apr 26, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 589992297 (NC_000023.11:119471776::T 3827/57605) Row 589992298 (NC_000023.11:119471776::TT 466/57959) Row 589992299 (NC_000023.11:119471776::TTT 19019/57539)...	-	Apr 26, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 589992297 (NC_000023.11:119471776::T 3827/57605) Row 589992298 (NC_000023.11:119471776::TT 466/57959) Row 589992299 (NC_000023.11:119471776::TTT 19019/57539)...	-	Apr 26, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 589992297 (NC_000023.11:119471776::T 3827/57605) Row 589992298 (NC_000023.11:119471776::TT 466/57959) Row 589992299 (NC_000023.11:119471776::TTT 19019/57539)...	-	Apr 26, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 589992297 (NC_000023.11:119471776::T 3827/57605) Row 589992298 (NC_000023.11:119471776::TT 466/57959) Row 589992299 (NC_000023.11:119471776::TTT 19019/57539)...	-	Apr 26, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 589992297 (NC_000023.11:119471776::T 3827/57605) Row 589992298 (NC_000023.11:119471776::TT 466/57959) Row 589992299 (NC_000023.11:119471776::TTT 19019/57539)...	-	Apr 26, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 589992297 (NC_000023.11:119471776::T 3827/57605) Row 589992298 (NC_000023.11:119471776::TT 466/57959) Row 589992299 (NC_000023.11:119471776::TTT 19019/57539)...	-	Apr 26, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 589992297 (NC_000023.11:119471776::T 3827/57605) Row 589992298 (NC_000023.11:119471776::TT 466/57959) Row 589992299 (NC_000023.11:119471776::TTT 19019/57539)...	-	Apr 26, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 589992297 (NC_000023.11:119471776::T 3827/57605) Row 589992298 (NC_000023.11:119471776::TT 466/57959) Row 589992299 (NC_000023.11:119471776::TTT 19019/57539)...	-	Apr 26, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 589992297 (NC_000023.11:119471776::T 3827/57605) Row 589992298 (NC_000023.11:119471776::TT 466/57959) Row 589992299 (NC_000023.11:119471776::TTT 19019/57539)...	-	Apr 26, 2021 (155)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 589992297 (NC_000023.11:119471776::T 3827/57605) Row 589992298 (NC_000023.11:119471776::TT 466/57959) Row 589992299 (NC_000023.11:119471776::TTT 19019/57539)...	-	Apr 26, 2021 (155)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 589992297 (NC_000023.11:119471776::T 3827/57605) Row 589992298 (NC_000023.11:119471776::TT 466/57959) Row 589992299 (NC_000023.11:119471776::TTT 19019/57539)...	-	Apr 26, 2021 (155)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 589992297 (NC_000023.11:119471776::T 3827/57605) Row 589992298 (NC_000023.11:119471776::TT 466/57959) Row 589992299 (NC_000023.11:119471776::TTT 19019/57539)...	-	Apr 26, 2021 (155)
83	gnomAD - Genomes Submission ignored due to conflicting rows: Row 589992297 (NC_000023.11:119471776::T 3827/57605) Row 589992298 (NC_000023.11:119471776::TT 466/57959) Row 589992299 (NC_000023.11:119471776::TTT 19019/57539)...	-	Apr 26, 2021 (155)
84	gnomAD - Genomes Submission ignored due to conflicting rows: Row 589992297 (NC_000023.11:119471776::T 3827/57605) Row 589992298 (NC_000023.11:119471776::TT 466/57959) Row 589992299 (NC_000023.11:119471776::TTT 19019/57539)...	-	Apr 26, 2021 (155)
85	gnomAD - Genomes Submission ignored due to conflicting rows: Row 589992297 (NC_000023.11:119471776::T 3827/57605) Row 589992298 (NC_000023.11:119471776::TT 466/57959) Row 589992299 (NC_000023.11:119471776::TTT 19019/57539)...	-	Apr 26, 2021 (155)
86	8.3KJPN Submission ignored due to conflicting rows: Row 94010604 (NC_000023.10:118605739::TTT 1892/12259) Row 94010605 (NC_000023.10:118605739:TTTTTTT: 149/12259) Row 94010606 (NC_000023.10:118605739::TTTT 720/12259)...	-	Apr 26, 2021 (155)
87	8.3KJPN Submission ignored due to conflicting rows: Row 94010604 (NC_000023.10:118605739::TTT 1892/12259) Row 94010605 (NC_000023.10:118605739:TTTTTTT: 149/12259) Row 94010606 (NC_000023.10:118605739::TTTT 720/12259)...	-	Apr 26, 2021 (155)
88	8.3KJPN Submission ignored due to conflicting rows: Row 94010604 (NC_000023.10:118605739::TTT 1892/12259) Row 94010605 (NC_000023.10:118605739:TTTTTTT: 149/12259) Row 94010606 (NC_000023.10:118605739::TTTT 720/12259)...	-	Apr 26, 2021 (155)
89	8.3KJPN Submission ignored due to conflicting rows: Row 94010604 (NC_000023.10:118605739::TTT 1892/12259) Row 94010605 (NC_000023.10:118605739:TTTTTTT: 149/12259) Row 94010606 (NC_000023.10:118605739::TTTT 720/12259)...	-	Apr 26, 2021 (155)
90	8.3KJPN Submission ignored due to conflicting rows: Row 94010604 (NC_000023.10:118605739::TTT 1892/12259) Row 94010605 (NC_000023.10:118605739:TTTTTTT: 149/12259) Row 94010606 (NC_000023.10:118605739::TTTT 720/12259)...	-	Apr 26, 2021 (155)
91	8.3KJPN Submission ignored due to conflicting rows: Row 94010604 (NC_000023.10:118605739::TTT 1892/12259) Row 94010605 (NC_000023.10:118605739:TTTTTTT: 149/12259) Row 94010606 (NC_000023.10:118605739::TTTT 720/12259)...	-	Apr 26, 2021 (155)
92	14KJPN Submission ignored due to conflicting rows: Row 132186842 (NC_000023.11:119471776:TTTTTTT: 310/19367) Row 132186843 (NC_000023.11:119471776::TTT 3324/19367) Row 132186844 (NC_000023.11:119471776::TTTT 1141/19367)...	-	Oct 17, 2022 (156)
93	14KJPN Submission ignored due to conflicting rows: Row 132186842 (NC_000023.11:119471776:TTTTTTT: 310/19367) Row 132186843 (NC_000023.11:119471776::TTT 3324/19367) Row 132186844 (NC_000023.11:119471776::TTTT 1141/19367)...	-	Oct 17, 2022 (156)
94	14KJPN Submission ignored due to conflicting rows: Row 132186842 (NC_000023.11:119471776:TTTTTTT: 310/19367) Row 132186843 (NC_000023.11:119471776::TTT 3324/19367) Row 132186844 (NC_000023.11:119471776::TTTT 1141/19367)...	-	Oct 17, 2022 (156)
95	14KJPN Submission ignored due to conflicting rows: Row 132186842 (NC_000023.11:119471776:TTTTTTT: 310/19367) Row 132186843 (NC_000023.11:119471776::TTT 3324/19367) Row 132186844 (NC_000023.11:119471776::TTTT 1141/19367)...	-	Oct 17, 2022 (156)
96	14KJPN Submission ignored due to conflicting rows: Row 132186842 (NC_000023.11:119471776:TTTTTTT: 310/19367) Row 132186843 (NC_000023.11:119471776::TTT 3324/19367) Row 132186844 (NC_000023.11:119471776::TTTT 1141/19367)...	-	Oct 17, 2022 (156)
97	14KJPN Submission ignored due to conflicting rows: Row 132186842 (NC_000023.11:119471776:TTTTTTT: 310/19367) Row 132186843 (NC_000023.11:119471776::TTT 3324/19367) Row 132186844 (NC_000023.11:119471776::TTTT 1141/19367)...	-	Oct 17, 2022 (156)
98	TopMed Submission ignored due to conflicting rows: Row 699117795 (NC_000023.11:119471776:TTTTTTTTTT: 6/264690) Row 699117796 (NC_000023.11:119471776:TTTTTTTTTTT: 10/264690) Row 699117797 (NC_000023.11:119471776:TTTTTTTTTTTT: 4/264690)...	-	Apr 26, 2021 (155)
99	TopMed Submission ignored due to conflicting rows: Row 699117795 (NC_000023.11:119471776:TTTTTTTTTT: 6/264690) Row 699117796 (NC_000023.11:119471776:TTTTTTTTTTT: 10/264690) Row 699117797 (NC_000023.11:119471776:TTTTTTTTTTTT: 4/264690)...	-	Apr 26, 2021 (155)
100	TopMed Submission ignored due to conflicting rows: Row 699117795 (NC_000023.11:119471776:TTTTTTTTTT: 6/264690) Row 699117796 (NC_000023.11:119471776:TTTTTTTTTTT: 10/264690) Row 699117797 (NC_000023.11:119471776:TTTTTTTTTTTT: 4/264690)...	-	Apr 26, 2021 (155)
101	TopMed Submission ignored due to conflicting rows: Row 699117795 (NC_000023.11:119471776:TTTTTTTTTT: 6/264690) Row 699117796 (NC_000023.11:119471776:TTTTTTTTTTT: 10/264690) Row 699117797 (NC_000023.11:119471776:TTTTTTTTTTTT: 4/264690)...	-	Apr 26, 2021 (155)
102	UK 10K study - Twins Submission ignored due to conflicting rows: Row 46217794 (NC_000023.10:118605739:TTTTTTTTTTTTTTTTTT: 334/3708) Row 46217795 (NC_000023.10:118605739::TTT 3374/3708)	-	Oct 12, 2018 (152)
103	UK 10K study - Twins Submission ignored due to conflicting rows: Row 46217794 (NC_000023.10:118605739:TTTTTTTTTTTTTTTTTT: 334/3708) Row 46217795 (NC_000023.10:118605739::TTT 3374/3708)	-	Oct 12, 2018 (152)
104	ALFA	NC_000023.11 - 119471777	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)
rs72305616	May 11, 2012 (137)
rs72321394	May 11, 2012 (137)
rs144830393	Sep 17, 2011 (135)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
835185557	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT	(self)
83893397, ss1555932653, ss1709838577, ss1709838807, ss3020535968	NC_000023.10:118605739:TTTTTTTTTTT… NC_000023.10:118605739:TTTTTTTTTTTTTTTTTT:	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
ss3066305925, ss3823337731, ss4377808690, ss5313743566, ss5505175438, ss5857182083	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTT:	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
835185557	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
ss194066978	NT_011786.16:2873449:TTTTTTTTTTTTT… NT_011786.16:2873449:TTTTTTTTTTTTTTTTTT:	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
ss103794487	NT_011786.16:2873459:TTTTTTTTTTTTT… NT_011786.16:2873459:TTTTTTTTTTTTTTTTTT:	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
ss4377808689	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTT:	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
835185557	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss4377808688	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTT:	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
835185557	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
835185557	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
835185557	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4377808687, ss5135511441	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTT:	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
835185557	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4377808686, ss5135511440	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTT:	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
835185557	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4377808685, ss5135511439	NC_000023.11:119471776:TTTTTTTTTTT:	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
835185557	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4377808684, ss5135511438	NC_000023.11:119471776:TTTTTTTTTT:	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
835185557	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4377808683	NC_000023.11:119471776:TTTTTTTTT:	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
835185557	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
835185557	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss5236041298	NC_000023.10:118605739:TTTTTTT:	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4377808682, ss5798349738	NC_000023.11:119471776:TTTTTTT:	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
835185557	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
835185557	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4377808681	NC_000023.11:119471776:TTTTT:	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
835185557	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4377808680	NC_000023.11:119471776:TTT:	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
835185557	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3836293770	NC_000023.10:118605739:TT:	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4377808679, ss5313743565, ss5505175436	NC_000023.11:119471776:TT:	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
835185557	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
	NC_000023.11:119471776:T:	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
835185557	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4309916	NT_011786.16:2873476:T:	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5236041301	NC_000023.10:118605739::T	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4377808668, ss5798349742	NC_000023.11:119471776::T	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
835185557	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5236041302	NC_000023.10:118605739::TT	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4377808669, ss5313743568, ss5798349743	NC_000023.11:119471776::TT	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
835185557	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss295462438	NC_000023.9:118489768::TTT	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5236041297	NC_000023.10:118605739::TTT	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss1710874701, ss1710874702	NC_000023.10:118605757::TTT	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4377808670, ss5505175437, ss5798349739	NC_000023.11:119471776::TTT	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
835185557	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4309916	NT_011786.16:2873476:T:TTTT	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5236041299	NC_000023.10:118605739::TTTT	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4377808671, ss5313743567, ss5798349740	NC_000023.11:119471776::TTTT	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
835185557	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5236041300	NC_000023.10:118605739::TTTTT	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4377808672, ss5798349741	NC_000023.11:119471776::TTTTT	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
835185557	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4377808673	NC_000023.11:119471776::TTTTTT	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
835185557	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4377808674	NC_000023.11:119471776::TTTTTTT	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4377808675	NC_000023.11:119471776::TTTTTTTT	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4377808676	NC_000023.11:119471776::TTTTTTTTT	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4377808677	NC_000023.11:119471776::TTTTTTTTTT	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI
ss3620608791	NC_000023.11:119471776:TTTTTT:	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT
ss3620608793	NC_000023.11:119471776:TTTTTTTT:	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT
ss3620608800	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTT:	NC_000023.11:119471776:TTTTTTTTTTT… NC_000023.11:119471776:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT

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

No publications for rs71820531

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

rs71820531