Name: rs766827269
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.

rs766827269

Current Build 156

Released September 21, 2022

Organism

Homo sapiens

Position

chrY:57070228-57070248 (GRCh38.p14)

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.

This SNP has mapping conflicts. See here for details.

Alleles

del(T)₁₂ / del(T)₁₀ / del(T)₆ / de…

del(T)₁₂ / del(T)₁₀ / del(T)₆ / del(T)₅ / del(T)₄ / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₅ / dup(T)₉

Variation Type

Indel Insertion and Deletion

Frequency

dupTTT=0.00605 (108/17860, ALFA)

delT=0.0148 (56/3775, 1000G)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: VAMP7 : Intron Variant
Publications: 0 citations
Genomic View: See rs on genome

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

Release Version: 20231103111315

Population	Group	Sample Size	Ref Allele	Alt Allele	Ref HMOZ	Alt HMOZ	HTRZ	HWEP
Total	Global	17860	TTTTTTTTTTTTTTTTTTTTT=0.98791	TTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTT=0.00095, TTTTTTTTTTTTTTTTTTTTTTTT=0.00605, TTTTTTTTTTTTTTTTTTTT=0.00157, TTTTTTTTTTTTTTTTTTTTTT=0.00207, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00095, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00050, TTTTTTTTTTTTTTTTTTTTTTT=0.00000	0.990487	0.002492	0.007022	32
European	Sub	13882	TTTTTTTTTTTTTTTTTTTTT=0.98444	TTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTT=0.00122, TTTTTTTTTTTTTTTTTTTTTTTT=0.00778, TTTTTTTTTTTTTTTTTTTT=0.00202, TTTTTTTTTTTTTTTTTTTTTT=0.00267, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00122, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00065, TTTTTTTTTTTTTTTTTTTTTTT=0.00000	0.987721	0.003216	0.009063	32
African	Sub	2570	TTTTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	86	TTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	2484	TTTTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	110	TTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
East Asian	Sub	84	TTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	26	TTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	134	TTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Latin American 2	Sub	592	TTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	98	TTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	474	TTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=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	17860	(T)₂₁=0.98791	del(T)₁₀=0.00000, del(T)₆=0.00000, del(T)₅=0.00000, del(T)₄=0.00000, delTT=0.00095, delT=0.00157, dupT=0.00207, dupTT=0.00000, dupTTT=0.00605, dup(T)₄=0.00050, dup(T)₅=0.00095
Allele Frequency Aggregator	European	Sub	13882	(T)₂₁=0.98444	del(T)₁₀=0.00000, del(T)₆=0.00000, del(T)₅=0.00000, del(T)₄=0.00000, delTT=0.00122, delT=0.00202, dupT=0.00267, dupTT=0.00000, dupTTT=0.00778, dup(T)₄=0.00065, dup(T)₅=0.00122
Allele Frequency Aggregator	African	Sub	2570	(T)₂₁=1.0000	del(T)₁₀=0.0000, del(T)₆=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000, dupTTT=0.0000, dup(T)₄=0.0000, dup(T)₅=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	592	(T)₂₁=1.000	del(T)₁₀=0.000, del(T)₆=0.000, del(T)₅=0.000, del(T)₄=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
Allele Frequency Aggregator	Other	Sub	474	(T)₂₁=1.000	del(T)₁₀=0.000, del(T)₆=0.000, del(T)₅=0.000, del(T)₄=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
Allele Frequency Aggregator	Latin American 1	Sub	134	(T)₂₁=1.000	del(T)₁₀=0.000, del(T)₆=0.000, del(T)₅=0.000, del(T)₄=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
Allele Frequency Aggregator	Asian	Sub	110	(T)₂₁=1.000	del(T)₁₀=0.000, del(T)₆=0.000, del(T)₅=0.000, del(T)₄=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
Allele Frequency Aggregator	South Asian	Sub	98	(T)₂₁=1.00	del(T)₁₀=0.00, del(T)₆=0.00, del(T)₅=0.00, del(T)₄=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
1000Genomes	Global	Study-wide	3775	(T)₂₁=0.9852	delT=0.0148
1000Genomes	African	Sub	1003	(T)₂₁=0.9771	delT=0.0229
1000Genomes	Europe	Sub	766	(T)₂₁=0.990	delT=0.010
1000Genomes	East Asian	Sub	764	(T)₂₁=0.986	delT=0.014
1000Genomes	South Asian	Sub	718	(T)₂₁=0.996	delT=0.004
1000Genomes	American	Sub	524	(T)₂₁=0.979	delT=0.021

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 Y	NC_000024.10:g.57070237_57070248del
GRCh38.p14 chr Y	NC_000024.10:g.57070239_57070248del
GRCh38.p14 chr Y	NC_000024.10:g.57070243_57070248del
GRCh38.p14 chr Y	NC_000024.10:g.57070244_57070248del
GRCh38.p14 chr Y	NC_000024.10:g.57070245_57070248del
GRCh38.p14 chr Y	NC_000024.10:g.57070247_57070248del
GRCh38.p14 chr Y	NC_000024.10:g.57070248del
GRCh38.p14 chr Y	NC_000024.10:g.57070248dup
GRCh38.p14 chr Y	NC_000024.10:g.57070247_57070248dup
GRCh38.p14 chr Y	NC_000024.10:g.57070246_57070248dup
GRCh38.p14 chr Y	NC_000024.10:g.57070245_57070248dup
GRCh38.p14 chr Y	NC_000024.10:g.57070244_57070248dup
GRCh38.p14 chr Y	NC_000024.10:g.57070240_57070248dup
GRCh37.p13 chr Y	NC_000024.9:g.59216386_59216397del
GRCh37.p13 chr Y	NC_000024.9:g.59216388_59216397del
GRCh37.p13 chr Y	NC_000024.9:g.59216392_59216397del
GRCh37.p13 chr Y	NC_000024.9:g.59216393_59216397del
GRCh37.p13 chr Y	NC_000024.9:g.59216394_59216397del
GRCh37.p13 chr Y	NC_000024.9:g.59216396_59216397del
GRCh37.p13 chr Y	NC_000024.9:g.59216397del
GRCh37.p13 chr Y	NC_000024.9:g.59216397dup
GRCh37.p13 chr Y	NC_000024.9:g.59216396_59216397dup
GRCh37.p13 chr Y	NC_000024.9:g.59216395_59216397dup
GRCh37.p13 chr Y	NC_000024.9:g.59216394_59216397dup
GRCh37.p13 chr Y	NC_000024.9:g.59216393_59216397dup
GRCh37.p13 chr Y	NC_000024.9:g.59216389_59216397dup
VAMP7 RefSeqGene	NG_021435.2:g.7374_7385del
VAMP7 RefSeqGene	NG_021435.2:g.7376_7385del
VAMP7 RefSeqGene	NG_021435.2:g.7380_7385del
VAMP7 RefSeqGene	NG_021435.2:g.7381_7385del
VAMP7 RefSeqGene	NG_021435.2:g.7382_7385del
VAMP7 RefSeqGene	NG_021435.2:g.7384_7385del
VAMP7 RefSeqGene	NG_021435.2:g.7385del
VAMP7 RefSeqGene	NG_021435.2:g.7385dup
VAMP7 RefSeqGene	NG_021435.2:g.7384_7385dup
VAMP7 RefSeqGene	NG_021435.2:g.7383_7385dup
VAMP7 RefSeqGene	NG_021435.2:g.7382_7385dup
VAMP7 RefSeqGene	NG_021435.2:g.7381_7385dup
VAMP7 RefSeqGene	NG_021435.2:g.7377_7385dup
VAMP7 RefSeqGene	NG_021435.1:g.7438_7449del
VAMP7 RefSeqGene	NG_021435.1:g.7440_7449del
VAMP7 RefSeqGene	NG_021435.1:g.7444_7449del
VAMP7 RefSeqGene	NG_021435.1:g.7445_7449del
VAMP7 RefSeqGene	NG_021435.1:g.7446_7449del
VAMP7 RefSeqGene	NG_021435.1:g.7448_7449del
VAMP7 RefSeqGene	NG_021435.1:g.7449del
VAMP7 RefSeqGene	NG_021435.1:g.7449dup
VAMP7 RefSeqGene	NG_021435.1:g.7448_7449dup
VAMP7 RefSeqGene	NG_021435.1:g.7447_7449dup
VAMP7 RefSeqGene	NG_021435.1:g.7446_7449dup
VAMP7 RefSeqGene	NG_021435.1:g.7445_7449dup
VAMP7 RefSeqGene	NG_021435.1:g.7441_7449dup
GRCh38.p14 chr X	NC_000023.11:g.155883717_155883728del
GRCh38.p14 chr X	NC_000023.11:g.155883719_155883728del
GRCh38.p14 chr X	NC_000023.11:g.155883723_155883728del
GRCh38.p14 chr X	NC_000023.11:g.155883724_155883728del
GRCh38.p14 chr X	NC_000023.11:g.155883725_155883728del
GRCh38.p14 chr X	NC_000023.11:g.155883727_155883728del
GRCh38.p14 chr X	NC_000023.11:g.155883728del
GRCh38.p14 chr X	NC_000023.11:g.155883728dup
GRCh38.p14 chr X	NC_000023.11:g.155883727_155883728dup
GRCh38.p14 chr X	NC_000023.11:g.155883726_155883728dup
GRCh38.p14 chr X	NC_000023.11:g.155883725_155883728dup
GRCh38.p14 chr X	NC_000023.11:g.155883724_155883728dup
GRCh38.p14 chr X	NC_000023.11:g.155883720_155883728dup
GRCh37.p13 chr X	NC_000023.10:g.155113380_155113391del
GRCh37.p13 chr X	NC_000023.10:g.155113382_155113391del
GRCh37.p13 chr X	NC_000023.10:g.155113386_155113391del
GRCh37.p13 chr X	NC_000023.10:g.155113387_155113391del
GRCh37.p13 chr X	NC_000023.10:g.155113388_155113391del
GRCh37.p13 chr X	NC_000023.10:g.155113390_155113391del
GRCh37.p13 chr X	NC_000023.10:g.155113391del
GRCh37.p13 chr X	NC_000023.10:g.155113391dup
GRCh37.p13 chr X	NC_000023.10:g.155113390_155113391dup
GRCh37.p13 chr X	NC_000023.10:g.155113389_155113391dup
GRCh37.p13 chr X	NC_000023.10:g.155113388_155113391dup
GRCh37.p13 chr X	NC_000023.10:g.155113387_155113391dup
GRCh37.p13 chr X	NC_000023.10:g.155113383_155113391dup

Gene: VAMP7, vesicle associated membrane protein 7 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
VAMP7 transcript variant 2	NM_001145149.3:c.-10+2269… NM_001145149.3:c.-10+2269_-10+2280del	N/A	Intron Variant
VAMP7 transcript variant 3	NM_001185183.2:c.-10+2269… NM_001185183.2:c.-10+2269_-10+2280del	N/A	Intron Variant
VAMP7 transcript variant 1	NM_005638.6:c.-10+2269_-1… NM_005638.6:c.-10+2269_-10+2280del	N/A	Intron Variant
VAMP7 transcript variant 4	NR_033714.2:n.	N/A	Intron Variant
VAMP7 transcript variant 5	NR_033715.2:n.	N/A	Intron Variant
VAMP7 transcript variant X1	XM_011531188.2:c.-172+226… XM_011531188.2:c.-172+2269_-172+2280del	N/A	Intron Variant
VAMP7 transcript variant X2	XM_017029760.2:c.-172+226… XM_017029760.2:c.-172+2269_-172+2280del	N/A	Intron Variant

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

Not Reported in ClinVar

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

Placement	(T)₂₁=	del(T)₁₂	del(T)₁₀	del(T)₆	del(T)₅	del(T)₄	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₅	dup(T)₉
GRCh38.p14 chr Y	NC_000024.10:g.57070228_57070248=	NC_000024.10:g.57070237_57070248del	NC_000024.10:g.57070239_57070248del	NC_000024.10:g.57070243_57070248del	NC_000024.10:g.57070244_57070248del	NC_000024.10:g.57070245_57070248del	NC_000024.10:g.57070247_57070248del	NC_000024.10:g.57070248del	NC_000024.10:g.57070248dup	NC_000024.10:g.57070247_57070248dup	NC_000024.10:g.57070246_57070248dup	NC_000024.10:g.57070245_57070248dup	NC_000024.10:g.57070244_57070248dup	NC_000024.10:g.57070240_57070248dup
GRCh37.p13 chr Y	NC_000024.9:g.59216377_59216397=	NC_000024.9:g.59216386_59216397del	NC_000024.9:g.59216388_59216397del	NC_000024.9:g.59216392_59216397del	NC_000024.9:g.59216393_59216397del	NC_000024.9:g.59216394_59216397del	NC_000024.9:g.59216396_59216397del	NC_000024.9:g.59216397del	NC_000024.9:g.59216397dup	NC_000024.9:g.59216396_59216397dup	NC_000024.9:g.59216395_59216397dup	NC_000024.9:g.59216394_59216397dup	NC_000024.9:g.59216393_59216397dup	NC_000024.9:g.59216389_59216397dup
VAMP7 RefSeqGene	NG_021435.2:g.7365_7385=	NG_021435.2:g.7374_7385del	NG_021435.2:g.7376_7385del	NG_021435.2:g.7380_7385del	NG_021435.2:g.7381_7385del	NG_021435.2:g.7382_7385del	NG_021435.2:g.7384_7385del	NG_021435.2:g.7385del	NG_021435.2:g.7385dup	NG_021435.2:g.7384_7385dup	NG_021435.2:g.7383_7385dup	NG_021435.2:g.7382_7385dup	NG_021435.2:g.7381_7385dup	NG_021435.2:g.7377_7385dup
VAMP7 RefSeqGene	NG_021435.1:g.7429_7449=	NG_021435.1:g.7438_7449del	NG_021435.1:g.7440_7449del	NG_021435.1:g.7444_7449del	NG_021435.1:g.7445_7449del	NG_021435.1:g.7446_7449del	NG_021435.1:g.7448_7449del	NG_021435.1:g.7449del	NG_021435.1:g.7449dup	NG_021435.1:g.7448_7449dup	NG_021435.1:g.7447_7449dup	NG_021435.1:g.7446_7449dup	NG_021435.1:g.7445_7449dup	NG_021435.1:g.7441_7449dup
GRCh38.p14 chr X	NC_000023.11:g.155883708_155883728=	NC_000023.11:g.155883717_155883728del	NC_000023.11:g.155883719_155883728del	NC_000023.11:g.155883723_155883728del	NC_000023.11:g.155883724_155883728del	NC_000023.11:g.155883725_155883728del	NC_000023.11:g.155883727_155883728del	NC_000023.11:g.155883728del	NC_000023.11:g.155883728dup	NC_000023.11:g.155883727_155883728dup	NC_000023.11:g.155883726_155883728dup	NC_000023.11:g.155883725_155883728dup	NC_000023.11:g.155883724_155883728dup	NC_000023.11:g.155883720_155883728dup
GRCh37.p13 chr X	NC_000023.10:g.155113371_155113391=	NC_000023.10:g.155113380_155113391del	NC_000023.10:g.155113382_155113391del	NC_000023.10:g.155113386_155113391del	NC_000023.10:g.155113387_155113391del	NC_000023.10:g.155113388_155113391del	NC_000023.10:g.155113390_155113391del	NC_000023.10:g.155113391del	NC_000023.10:g.155113391dup	NC_000023.10:g.155113390_155113391dup	NC_000023.10:g.155113389_155113391dup	NC_000023.10:g.155113388_155113391dup	NC_000023.10:g.155113387_155113391dup	NC_000023.10:g.155113383_155113391dup
VAMP7 transcript variant 2	NM_001145149.2:c.-10+2260=	NM_001145149.2:c.-10+2269_-10+2280del	NM_001145149.2:c.-10+2271_-10+2280del	NM_001145149.2:c.-10+2275_-10+2280del	NM_001145149.2:c.-10+2276_-10+2280del	NM_001145149.2:c.-10+2277_-10+2280del	NM_001145149.2:c.-10+2279_-10+2280del	NM_001145149.2:c.-10+2280del	NM_001145149.2:c.-10+2280dup	NM_001145149.2:c.-10+2279_-10+2280dup	NM_001145149.2:c.-10+2278_-10+2280dup	NM_001145149.2:c.-10+2277_-10+2280dup	NM_001145149.2:c.-10+2276_-10+2280dup	NM_001145149.2:c.-10+2272_-10+2280dup
VAMP7 transcript variant 2	NM_001145149.3:c.-10+2260=	NM_001145149.3:c.-10+2269_-10+2280del	NM_001145149.3:c.-10+2271_-10+2280del	NM_001145149.3:c.-10+2275_-10+2280del	NM_001145149.3:c.-10+2276_-10+2280del	NM_001145149.3:c.-10+2277_-10+2280del	NM_001145149.3:c.-10+2279_-10+2280del	NM_001145149.3:c.-10+2280del	NM_001145149.3:c.-10+2280dup	NM_001145149.3:c.-10+2279_-10+2280dup	NM_001145149.3:c.-10+2278_-10+2280dup	NM_001145149.3:c.-10+2277_-10+2280dup	NM_001145149.3:c.-10+2276_-10+2280dup	NM_001145149.3:c.-10+2272_-10+2280dup
VAMP7 transcript variant 3	NM_001185183.1:c.-10+2260=	NM_001185183.1:c.-10+2269_-10+2280del	NM_001185183.1:c.-10+2271_-10+2280del	NM_001185183.1:c.-10+2275_-10+2280del	NM_001185183.1:c.-10+2276_-10+2280del	NM_001185183.1:c.-10+2277_-10+2280del	NM_001185183.1:c.-10+2279_-10+2280del	NM_001185183.1:c.-10+2280del	NM_001185183.1:c.-10+2280dup	NM_001185183.1:c.-10+2279_-10+2280dup	NM_001185183.1:c.-10+2278_-10+2280dup	NM_001185183.1:c.-10+2277_-10+2280dup	NM_001185183.1:c.-10+2276_-10+2280dup	NM_001185183.1:c.-10+2272_-10+2280dup
VAMP7 transcript variant 3	NM_001185183.2:c.-10+2260=	NM_001185183.2:c.-10+2269_-10+2280del	NM_001185183.2:c.-10+2271_-10+2280del	NM_001185183.2:c.-10+2275_-10+2280del	NM_001185183.2:c.-10+2276_-10+2280del	NM_001185183.2:c.-10+2277_-10+2280del	NM_001185183.2:c.-10+2279_-10+2280del	NM_001185183.2:c.-10+2280del	NM_001185183.2:c.-10+2280dup	NM_001185183.2:c.-10+2279_-10+2280dup	NM_001185183.2:c.-10+2278_-10+2280dup	NM_001185183.2:c.-10+2277_-10+2280dup	NM_001185183.2:c.-10+2276_-10+2280dup	NM_001185183.2:c.-10+2272_-10+2280dup
VAMP7 transcript variant 1	NM_005638.5:c.-10+2260=	NM_005638.5:c.-10+2269_-10+2280del	NM_005638.5:c.-10+2271_-10+2280del	NM_005638.5:c.-10+2275_-10+2280del	NM_005638.5:c.-10+2276_-10+2280del	NM_005638.5:c.-10+2277_-10+2280del	NM_005638.5:c.-10+2279_-10+2280del	NM_005638.5:c.-10+2280del	NM_005638.5:c.-10+2280dup	NM_005638.5:c.-10+2279_-10+2280dup	NM_005638.5:c.-10+2278_-10+2280dup	NM_005638.5:c.-10+2277_-10+2280dup	NM_005638.5:c.-10+2276_-10+2280dup	NM_005638.5:c.-10+2272_-10+2280dup
VAMP7 transcript variant 1	NM_005638.6:c.-10+2260=	NM_005638.6:c.-10+2269_-10+2280del	NM_005638.6:c.-10+2271_-10+2280del	NM_005638.6:c.-10+2275_-10+2280del	NM_005638.6:c.-10+2276_-10+2280del	NM_005638.6:c.-10+2277_-10+2280del	NM_005638.6:c.-10+2279_-10+2280del	NM_005638.6:c.-10+2280del	NM_005638.6:c.-10+2280dup	NM_005638.6:c.-10+2279_-10+2280dup	NM_005638.6:c.-10+2278_-10+2280dup	NM_005638.6:c.-10+2277_-10+2280dup	NM_005638.6:c.-10+2276_-10+2280dup	NM_005638.6:c.-10+2272_-10+2280dup
VAMP7 transcript variant X1	XM_011531188.2:c.-172+2260=	XM_011531188.2:c.-172+2269_-172+2280del	XM_011531188.2:c.-172+2271_-172+2280del	XM_011531188.2:c.-172+2275_-172+2280del	XM_011531188.2:c.-172+2276_-172+2280del	XM_011531188.2:c.-172+2277_-172+2280del	XM_011531188.2:c.-172+2279_-172+2280del	XM_011531188.2:c.-172+2280del	XM_011531188.2:c.-172+2280dup	XM_011531188.2:c.-172+2279_-172+2280dup	XM_011531188.2:c.-172+2278_-172+2280dup	XM_011531188.2:c.-172+2277_-172+2280dup	XM_011531188.2:c.-172+2276_-172+2280dup	XM_011531188.2:c.-172+2272_-172+2280dup
VAMP7 transcript variant X1	XM_011545653.2:c.-172+2260=	XM_011545653.2:c.-172+2269_-172+2280del	XM_011545653.2:c.-172+2271_-172+2280del	XM_011545653.2:c.-172+2275_-172+2280del	XM_011545653.2:c.-172+2276_-172+2280del	XM_011545653.2:c.-172+2277_-172+2280del	XM_011545653.2:c.-172+2279_-172+2280del	XM_011545653.2:c.-172+2280del	XM_011545653.2:c.-172+2280dup	XM_011545653.2:c.-172+2279_-172+2280dup	XM_011545653.2:c.-172+2278_-172+2280dup	XM_011545653.2:c.-172+2277_-172+2280dup	XM_011545653.2:c.-172+2276_-172+2280dup	XM_011545653.2:c.-172+2272_-172+2280dup
VAMP7 transcript variant X2	XM_017029760.2:c.-172+2260=	XM_017029760.2:c.-172+2269_-172+2280del	XM_017029760.2:c.-172+2271_-172+2280del	XM_017029760.2:c.-172+2275_-172+2280del	XM_017029760.2:c.-172+2276_-172+2280del	XM_017029760.2:c.-172+2277_-172+2280del	XM_017029760.2:c.-172+2279_-172+2280del	XM_017029760.2:c.-172+2280del	XM_017029760.2:c.-172+2280dup	XM_017029760.2:c.-172+2279_-172+2280dup	XM_017029760.2:c.-172+2278_-172+2280dup	XM_017029760.2:c.-172+2277_-172+2280dup	XM_017029760.2:c.-172+2276_-172+2280dup	XM_017029760.2:c.-172+2272_-172+2280dup
VAMP7 transcript variant X2	XM_017030063.2:c.-172+2260=	XM_017030063.2:c.-172+2269_-172+2280del	XM_017030063.2:c.-172+2271_-172+2280del	XM_017030063.2:c.-172+2275_-172+2280del	XM_017030063.2:c.-172+2276_-172+2280del	XM_017030063.2:c.-172+2277_-172+2280del	XM_017030063.2:c.-172+2279_-172+2280del	XM_017030063.2:c.-172+2280del	XM_017030063.2:c.-172+2280dup	XM_017030063.2:c.-172+2279_-172+2280dup	XM_017030063.2:c.-172+2278_-172+2280dup	XM_017030063.2:c.-172+2277_-172+2280dup	XM_017030063.2:c.-172+2276_-172+2280dup	XM_017030063.2:c.-172+2272_-172+2280dup

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#.

30 SubSNP, 21 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	1000GENOMES	ss1556722890	Apr 01, 2015 (144)
2	SWEGEN	ss3020835684	Jan 10, 2018 (151)
3	EVA	ss3836369896	Apr 27, 2020 (154)
4	GNOMAD	ss4125895250	Apr 26, 2021 (155)
5	GNOMAD	ss4125895251	Apr 26, 2021 (155)
6	GNOMAD	ss4125895252	Apr 26, 2021 (155)
7	GNOMAD	ss4125895253	Apr 26, 2021 (155)
8	GNOMAD	ss4125895254	Apr 26, 2021 (155)
9	GNOMAD	ss4125895255	Apr 26, 2021 (155)
10	GNOMAD	ss4125895256	Apr 26, 2021 (155)
11	GNOMAD	ss4125895257	Apr 26, 2021 (155)
12	GNOMAD	ss4125895258	Apr 26, 2021 (155)
13	TOPMED	ss5141827898	Apr 26, 2021 (155)
14	TOPMED	ss5141827899	Apr 26, 2021 (155)
15	TOMMO_GENOMICS	ss5236843690	Apr 26, 2021 (155)
16	TOMMO_GENOMICS	ss5236843691	Apr 26, 2021 (155)
17	TOMMO_GENOMICS	ss5236843692	Apr 26, 2021 (155)
18	TOMMO_GENOMICS	ss5236843693	Apr 26, 2021 (155)
19	1000G_HIGH_COVERAGE	ss5314384316	Oct 13, 2022 (156)
20	1000G_HIGH_COVERAGE	ss5314384317	Oct 13, 2022 (156)
21	1000G_HIGH_COVERAGE	ss5314384318	Oct 13, 2022 (156)
22	HUGCELL_USP	ss5505732199	Oct 13, 2022 (156)
23	HUGCELL_USP	ss5505732200	Oct 13, 2022 (156)
24	HUGCELL_USP	ss5505732201	Oct 13, 2022 (156)
25	HUGCELL_USP	ss5505732202	Oct 13, 2022 (156)
26	HUGCELL_USP	ss5505732203	Oct 13, 2022 (156)
27	TOMMO_GENOMICS	ss5799389737	Oct 13, 2022 (156)
28	TOMMO_GENOMICS	ss5799389738	Oct 13, 2022 (156)
29	TOMMO_GENOMICS	ss5799389739	Oct 13, 2022 (156)
30	TOMMO_GENOMICS	ss5799389740	Oct 13, 2022 (156)
31	1000Genomes	NC_000023.10 - 155113371	Oct 12, 2018 (152)
32	gnomAD - Genomes Submission ignored due to conflicting rows: Row 594728630 (NC_000023.11:155883707::TT 428/115194) Row 594728631 (NC_000023.11:155883707::TTT 100/115254) Row 594728632 (NC_000023.11:155883707::TTTT 12/115260)...	-	Apr 26, 2021 (155)
33	gnomAD - Genomes Submission ignored due to conflicting rows: Row 594728630 (NC_000023.11:155883707::TT 428/115194) Row 594728631 (NC_000023.11:155883707::TTT 100/115254) Row 594728632 (NC_000023.11:155883707::TTTT 12/115260)...	-	Apr 26, 2021 (155)
34	gnomAD - Genomes Submission ignored due to conflicting rows: Row 594728630 (NC_000023.11:155883707::TT 428/115194) Row 594728631 (NC_000023.11:155883707::TTT 100/115254) Row 594728632 (NC_000023.11:155883707::TTTT 12/115260)...	-	Apr 26, 2021 (155)
35	gnomAD - Genomes Submission ignored due to conflicting rows: Row 594728630 (NC_000023.11:155883707::TT 428/115194) Row 594728631 (NC_000023.11:155883707::TTT 100/115254) Row 594728632 (NC_000023.11:155883707::TTTT 12/115260)...	-	Apr 26, 2021 (155)
36	gnomAD - Genomes Submission ignored due to conflicting rows: Row 594728630 (NC_000023.11:155883707::TT 428/115194) Row 594728631 (NC_000023.11:155883707::TTT 100/115254) Row 594728632 (NC_000023.11:155883707::TTTT 12/115260)...	-	Apr 26, 2021 (155)
37	gnomAD - Genomes Submission ignored due to conflicting rows: Row 594728630 (NC_000023.11:155883707::TT 428/115194) Row 594728631 (NC_000023.11:155883707::TTT 100/115254) Row 594728632 (NC_000023.11:155883707::TTTT 12/115260)...	-	Apr 26, 2021 (155)
38	gnomAD - Genomes Submission ignored due to conflicting rows: Row 594728630 (NC_000023.11:155883707::TT 428/115194) Row 594728631 (NC_000023.11:155883707::TTT 100/115254) Row 594728632 (NC_000023.11:155883707::TTTT 12/115260)...	-	Apr 26, 2021 (155)
39	gnomAD - Genomes Submission ignored due to conflicting rows: Row 594728630 (NC_000023.11:155883707::TT 428/115194) Row 594728631 (NC_000023.11:155883707::TTT 100/115254) Row 594728632 (NC_000023.11:155883707::TTTT 12/115260)...	-	Apr 26, 2021 (155)
40	gnomAD - Genomes Submission ignored due to conflicting rows: Row 594728630 (NC_000023.11:155883707::TT 428/115194) Row 594728631 (NC_000023.11:155883707::TTT 100/115254) Row 594728632 (NC_000023.11:155883707::TTTT 12/115260)...	-	Apr 26, 2021 (155)
41	8.3KJPN Submission ignored due to conflicting rows: Row 94812997 (NC_000023.10:155113370::T 55/16760) Row 94812998 (NC_000023.10:155113370:T: 19/16760) Row 94812999 (NC_000023.10:155113370:TTTTTTTTTTTT: 1/16760)...	-	Apr 26, 2021 (155)
42	8.3KJPN Submission ignored due to conflicting rows: Row 94812997 (NC_000023.10:155113370::T 55/16760) Row 94812998 (NC_000023.10:155113370:T: 19/16760) Row 94812999 (NC_000023.10:155113370:TTTTTTTTTTTT: 1/16760)...	-	Apr 26, 2021 (155)
43	8.3KJPN Submission ignored due to conflicting rows: Row 94812997 (NC_000023.10:155113370::T 55/16760) Row 94812998 (NC_000023.10:155113370:T: 19/16760) Row 94812999 (NC_000023.10:155113370:TTTTTTTTTTTT: 1/16760)...	-	Apr 26, 2021 (155)
44	8.3KJPN Submission ignored due to conflicting rows: Row 94812997 (NC_000023.10:155113370::T 55/16760) Row 94812998 (NC_000023.10:155113370:T: 19/16760) Row 94812999 (NC_000023.10:155113370:TTTTTTTTTTTT: 1/16760)...	-	Apr 26, 2021 (155)
45	14KJPN Submission ignored due to conflicting rows: Row 133226841 (NC_000023.11:155883707:T: 36/28256) Row 133226842 (NC_000023.11:155883707::T 94/28256) Row 133226843 (NC_000023.11:155883707:TTTTTTTTTTTT: 1/28256)...	-	Oct 13, 2022 (156)
46	14KJPN Submission ignored due to conflicting rows: Row 133226841 (NC_000023.11:155883707:T: 36/28256) Row 133226842 (NC_000023.11:155883707::T 94/28256) Row 133226843 (NC_000023.11:155883707:TTTTTTTTTTTT: 1/28256)...	-	Oct 13, 2022 (156)
47	14KJPN Submission ignored due to conflicting rows: Row 133226841 (NC_000023.11:155883707:T: 36/28256) Row 133226842 (NC_000023.11:155883707::T 94/28256) Row 133226843 (NC_000023.11:155883707:TTTTTTTTTTTT: 1/28256)...	-	Oct 13, 2022 (156)
48	14KJPN Submission ignored due to conflicting rows: Row 133226841 (NC_000023.11:155883707:T: 36/28256) Row 133226842 (NC_000023.11:155883707::T 94/28256) Row 133226843 (NC_000023.11:155883707:TTTTTTTTTTTT: 1/28256)...	-	Oct 13, 2022 (156)
49	TopMed Submission ignored due to conflicting rows: Row 705434255 (NC_000023.11:155883707:TTTTTT: 1/264690) Row 705434256 (NC_000023.11:155883707:TTTTTTTTTT: 1/264690)	-	Apr 26, 2021 (155)
50	TopMed Submission ignored due to conflicting rows: Row 705434255 (NC_000023.11:155883707:TTTTTT: 1/264690) Row 705434256 (NC_000023.11:155883707:TTTTTTTTTT: 1/264690)	-	Apr 26, 2021 (155)
51	ALFA	NC_000024.10 - 57070228	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
ss5236843692	NC_000023.10:155113370:TTTTTTTTTTT… NC_000023.10:155113370:TTTTTTTTTTTT:	NC_000024.10:57070227:TTTTTTTTTTTT… NC_000024.10:57070227:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT	(self)
ss5799389739	NC_000023.11:155883707:TTTTTTTTTTT… NC_000023.11:155883707:TTTTTTTTTTTT:	NC_000024.10:57070227:TTTTTTTTTTTT… NC_000024.10:57070227:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT
ss5141827899	NC_000023.11:155883707:TTTTTTTTTT:	NC_000024.10:57070227:TTTTTTTTTTTT… NC_000024.10:57070227:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
12413458567	NC_000024.10:57070227:TTTTTTTTTTTT… NC_000024.10:57070227:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	NC_000024.10:57070227:TTTTTTTTTTTT… NC_000024.10:57070227:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss4125895258, ss5141827898	NC_000023.11:155883707:TTTTTT:	NC_000024.10:57070227:TTTTTTTTTTTT… NC_000024.10:57070227:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
12413458567	NC_000024.10:57070227:TTTTTTTTTTTT… NC_000024.10:57070227:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000024.10:57070227:TTTTTTTTTTTT… NC_000024.10:57070227:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4125895257	NC_000023.11:155883707:TTTTT:	NC_000024.10:57070227:TTTTTTTTTTTT… NC_000024.10:57070227:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
12413458567	NC_000024.10:57070227:TTTTTTTTTTTT… NC_000024.10:57070227:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000024.10:57070227:TTTTTTTTTTTT… NC_000024.10:57070227:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4125895256, ss5505732203	NC_000023.11:155883707:TTTT:	NC_000024.10:57070227:TTTTTTTTTTTT… NC_000024.10:57070227:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
12413458567	NC_000024.10:57070227:TTTTTTTTTTTT… NC_000024.10:57070227:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000024.10:57070227:TTTTTTTTTTTT… NC_000024.10:57070227:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss3020835684, ss5236843693	NC_000023.10:155113370:TT:	NC_000024.10:57070227:TTTTTTTTTTTT… NC_000024.10:57070227:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4125895255, ss5314384317, ss5505732200, ss5799389740	NC_000023.11:155883707:TT:	NC_000024.10:57070227:TTTTTTTTTTTT… NC_000024.10:57070227:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
12413458567	NC_000024.10:57070227:TTTTTTTTTTTT… NC_000024.10:57070227:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000024.10:57070227:TTTTTTTTTTTT… NC_000024.10:57070227:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
84675920, ss1556722890, ss5236843691	NC_000023.10:155113370:T:	NC_000024.10:57070227:TTTTTTTTTTTT… NC_000024.10:57070227:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4125895254, ss5314384316, ss5505732199, ss5799389737	NC_000023.11:155883707:T:	NC_000024.10:57070227:TTTTTTTTTTTT… NC_000024.10:57070227:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
12413458567	NC_000024.10:57070227:TTTTTTTTTTTT… NC_000024.10:57070227:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000024.10:57070227:TTTTTTTTTTTT… NC_000024.10:57070227:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss3836369896, ss5236843690	NC_000023.10:155113370::T	NC_000024.10:57070227:TTTTTTTTTTTT… NC_000024.10:57070227:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss5314384318, ss5505732201, ss5799389738	NC_000023.11:155883707::T	NC_000024.10:57070227:TTTTTTTTTTTT… NC_000024.10:57070227:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
12413458567	NC_000024.10:57070227:TTTTTTTTTTTT… NC_000024.10:57070227:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000024.10:57070227:TTTTTTTTTTTT… NC_000024.10:57070227:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4125895250, ss5505732202	NC_000023.11:155883707::TT	NC_000024.10:57070227:TTTTTTTTTTTT… NC_000024.10:57070227:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
12413458567	NC_000024.10:57070227:TTTTTTTTTTTT… NC_000024.10:57070227:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000024.10:57070227:TTTTTTTTTTTT… NC_000024.10:57070227:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4125895251	NC_000023.11:155883707::TTT	NC_000024.10:57070227:TTTTTTTTTTTT… NC_000024.10:57070227:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
12413458567	NC_000024.10:57070227:TTTTTTTTTTTT… NC_000024.10:57070227:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000024.10:57070227:TTTTTTTTTTTT… NC_000024.10:57070227:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4125895252	NC_000023.11:155883707::TTTT	NC_000024.10:57070227:TTTTTTTTTTTT… NC_000024.10:57070227:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
12413458567	NC_000024.10:57070227:TTTTTTTTTTTT… NC_000024.10:57070227:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000024.10:57070227:TTTTTTTTTTTT… NC_000024.10:57070227:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
12413458567	NC_000024.10:57070227:TTTTTTTTTTTT… NC_000024.10:57070227:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000024.10:57070227:TTTTTTTTTTTT… NC_000024.10:57070227:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4125895253	NC_000023.11:155883707::TTTTTTTTT	NC_000024.10:57070227:TTTTTTTTTTTT… NC_000024.10:57070227:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)

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

No publications for rs766827269

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

Genome context:

Select flank length:

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

Choose placement

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs766827269