Name: rs764981282
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.

rs764981282

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr3:6715693-6715706 (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)₅ / del(T)₄ / delTTT / delTT…
del(T)₅ / del(T)₄ / 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 / dup(T)₁₁ / dup(T)₁₃
Variation Type: Indel Insertion and Deletion
Frequency: del(T)₅=0.0000 (0/8576, ALFA)
del(T)₄=0.0000 (0/8576, ALFA)
delTTT=0.0000 (0/8576, ALFA) (+ 10 more)
delTT=0.0000 (0/8576, ALFA)
delT=0.0000 (0/8576, ALFA)
dupT=0.0000 (0/8576, ALFA)
dupTT=0.0000 (0/8576, ALFA)
dupTTT=0.0000 (0/8576, ALFA)
dup(T)₄=0.0000 (0/8576, ALFA)
dup(T)₅=0.0000 (0/8576, ALFA)
dup(T)₆=0.0000 (0/8576, ALFA)
dup(T)₁₁=0.0000 (0/8576, ALFA)
dupT=0.079 (46/582, NorthernSweden)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: GRM7-AS3 : Intron Variant
LOC105376944 : 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	8576	TTTTTTTTTTTTTT=1.0000	TTTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
European	Sub	5866	TTTTTTTTTTTTTT=1.0000	TTTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
African	Sub	1648	TTTTTTTTTTTTTT=1.0000	TTTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
African Others	Sub	60	TTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
African American	Sub	1588	TTTTTTTTTTTTTT=1.0000	TTTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
Asian	Sub	50	TTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
East Asian	Sub	36	TTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Other Asian	Sub	14	TTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Latin American 1	Sub	114	TTTTTTTTTTTTTT=1.000	TTTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	N/A
Latin American 2	Sub	494	TTTTTTTTTTTTTT=1.000	TTTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	N/A
South Asian	Sub	66	TTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Other	Sub	338	TTTTTTTTTTTTTT=1.000	TTTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=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
Allele Frequency Aggregator	Total	Global	8576	(T)₁₄=1.0000	del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000, dupTTT=0.0000, dup(T)₄=0.0000, dup(T)₅=0.0000, dup(T)₆=0.0000, dup(T)₁₁=0.0000
Allele Frequency Aggregator	European	Sub	5866	(T)₁₄=1.0000	del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000, dupTTT=0.0000, dup(T)₄=0.0000, dup(T)₅=0.0000, dup(T)₆=0.0000, dup(T)₁₁=0.0000
Allele Frequency Aggregator	African	Sub	1648	(T)₁₄=1.0000	del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000, dupTTT=0.0000, dup(T)₄=0.0000, dup(T)₅=0.0000, dup(T)₆=0.0000, dup(T)₁₁=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	494	(T)₁₄=1.000	del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₅=0.000, dup(T)₆=0.000, dup(T)₁₁=0.000
Allele Frequency Aggregator	Other	Sub	338	(T)₁₄=1.000	del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₅=0.000, dup(T)₆=0.000, dup(T)₁₁=0.000
Allele Frequency Aggregator	Latin American 1	Sub	114	(T)₁₄=1.000	del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₅=0.000, dup(T)₆=0.000, dup(T)₁₁=0.000
Allele Frequency Aggregator	South Asian	Sub	66	(T)₁₄=1.00	del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₅=0.00, dup(T)₆=0.00, dup(T)₁₁=0.00
Allele Frequency Aggregator	Asian	Sub	50	(T)₁₄=1.00	del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₅=0.00, dup(T)₆=0.00, dup(T)₁₁=0.00
Northern Sweden	ACPOP	Study-wide	582	- No frequency provided	dupT=0.079

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 3	NC_000003.12:g.6715702_6715706del
GRCh38.p14 chr 3	NC_000003.12:g.6715703_6715706del
GRCh38.p14 chr 3	NC_000003.12:g.6715704_6715706del
GRCh38.p14 chr 3	NC_000003.12:g.6715705_6715706del
GRCh38.p14 chr 3	NC_000003.12:g.6715706del
GRCh38.p14 chr 3	NC_000003.12:g.6715706dup
GRCh38.p14 chr 3	NC_000003.12:g.6715705_6715706dup
GRCh38.p14 chr 3	NC_000003.12:g.6715704_6715706dup
GRCh38.p14 chr 3	NC_000003.12:g.6715703_6715706dup
GRCh38.p14 chr 3	NC_000003.12:g.6715702_6715706dup
GRCh38.p14 chr 3	NC_000003.12:g.6715701_6715706dup
GRCh38.p14 chr 3	NC_000003.12:g.6715700_6715706dup
GRCh38.p14 chr 3	NC_000003.12:g.6715699_6715706dup
GRCh38.p14 chr 3	NC_000003.12:g.6715698_6715706dup
GRCh38.p14 chr 3	NC_000003.12:g.6715697_6715706dup
GRCh38.p14 chr 3	NC_000003.12:g.6715696_6715706dup
GRCh38.p14 chr 3	NC_000003.12:g.6715694_6715706dup
GRCh37.p13 chr 3	NC_000003.11:g.6757389_6757393del
GRCh37.p13 chr 3	NC_000003.11:g.6757390_6757393del
GRCh37.p13 chr 3	NC_000003.11:g.6757391_6757393del
GRCh37.p13 chr 3	NC_000003.11:g.6757392_6757393del
GRCh37.p13 chr 3	NC_000003.11:g.6757393del
GRCh37.p13 chr 3	NC_000003.11:g.6757393dup
GRCh37.p13 chr 3	NC_000003.11:g.6757392_6757393dup
GRCh37.p13 chr 3	NC_000003.11:g.6757391_6757393dup
GRCh37.p13 chr 3	NC_000003.11:g.6757390_6757393dup
GRCh37.p13 chr 3	NC_000003.11:g.6757389_6757393dup
GRCh37.p13 chr 3	NC_000003.11:g.6757388_6757393dup
GRCh37.p13 chr 3	NC_000003.11:g.6757387_6757393dup
GRCh37.p13 chr 3	NC_000003.11:g.6757386_6757393dup
GRCh37.p13 chr 3	NC_000003.11:g.6757385_6757393dup
GRCh37.p13 chr 3	NC_000003.11:g.6757384_6757393dup
GRCh37.p13 chr 3	NC_000003.11:g.6757383_6757393dup
GRCh37.p13 chr 3	NC_000003.11:g.6757381_6757393dup

Gene: GRM7-AS3, GRM7 antisense RNA 3 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
GRM7-AS3 transcript variant 1	NR_110123.1:n.	N/A	Intron Variant
GRM7-AS3 transcript variant 2	NR_110125.1:n.	N/A	Genic Downstream Transcript Variant

Gene: LOC105376944, uncharacterized LOC105376944 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LOC105376944 transcript variant X5	XR_001740417.1:n.	N/A	Intron Variant
LOC105376944 transcript variant X10	XR_001740418.1:n.	N/A	Intron Variant
LOC105376944 transcript variant X2	XR_002959674.1:n.	N/A	Intron Variant
LOC105376944 transcript variant X1	XR_007095802.1:n.	N/A	Intron Variant
LOC105376944 transcript variant X3	XR_007095803.1:n.	N/A	Intron Variant
LOC105376944 transcript variant X4	XR_007095804.1:n.	N/A	Intron Variant
LOC105376944 transcript variant X6	XR_007095805.1:n.	N/A	Intron Variant
LOC105376944 transcript variant X7	XR_007095806.1:n.	N/A	Intron Variant
LOC105376944 transcript variant X8	XR_007095807.1:n.	N/A	Intron Variant
LOC105376944 transcript variant X9	XR_007095808.1:n.	N/A	Intron Variant
LOC105376944 transcript variant X11	XR_007095809.1:n.	N/A	Intron Variant
LOC105376944 transcript variant X12	XR_007095810.1:n.	N/A	Intron Variant
LOC105376944 transcript variant X13	XR_007095811.1:n.	N/A	Intron Variant

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

Not Reported in ClinVar

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

Placement	(T)₁₄=	del(T)₅	del(T)₄	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	dup(T)₁₁	dup(T)₁₃
GRCh38.p14 chr 3	NC_000003.12:g.6715693_6715706=	NC_000003.12:g.6715702_6715706del	NC_000003.12:g.6715703_6715706del	NC_000003.12:g.6715704_6715706del	NC_000003.12:g.6715705_6715706del	NC_000003.12:g.6715706del	NC_000003.12:g.6715706dup	NC_000003.12:g.6715705_6715706dup	NC_000003.12:g.6715704_6715706dup	NC_000003.12:g.6715703_6715706dup	NC_000003.12:g.6715702_6715706dup	NC_000003.12:g.6715701_6715706dup	NC_000003.12:g.6715700_6715706dup	NC_000003.12:g.6715699_6715706dup	NC_000003.12:g.6715698_6715706dup	NC_000003.12:g.6715697_6715706dup	NC_000003.12:g.6715696_6715706dup	NC_000003.12:g.6715694_6715706dup
GRCh37.p13 chr 3	NC_000003.11:g.6757380_6757393=	NC_000003.11:g.6757389_6757393del	NC_000003.11:g.6757390_6757393del	NC_000003.11:g.6757391_6757393del	NC_000003.11:g.6757392_6757393del	NC_000003.11:g.6757393del	NC_000003.11:g.6757393dup	NC_000003.11:g.6757392_6757393dup	NC_000003.11:g.6757391_6757393dup	NC_000003.11:g.6757390_6757393dup	NC_000003.11:g.6757389_6757393dup	NC_000003.11:g.6757388_6757393dup	NC_000003.11:g.6757387_6757393dup	NC_000003.11:g.6757386_6757393dup	NC_000003.11:g.6757385_6757393dup	NC_000003.11:g.6757384_6757393dup	NC_000003.11:g.6757383_6757393dup	NC_000003.11:g.6757381_6757393dup

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#.

27 SubSNP, 24 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	SSMP	ss663422391	Apr 01, 2015 (144)
2	EVA_DECODE	ss3708565117	Jul 13, 2019 (153)
3	EVA_DECODE	ss3708565118	Jul 13, 2019 (153)
4	ACPOP	ss3729600085	Jul 13, 2019 (153)
5	KOGIC	ss3950592774	Apr 25, 2020 (154)
6	KOGIC	ss3950592775	Apr 25, 2020 (154)
7	KOGIC	ss3950592776	Apr 25, 2020 (154)
8	GNOMAD	ss4065257054	Apr 26, 2021 (155)
9	GNOMAD	ss4065257135	Apr 26, 2021 (155)
10	GNOMAD	ss4065257136	Apr 26, 2021 (155)
11	GNOMAD	ss4065257137	Apr 26, 2021 (155)
12	GNOMAD	ss4065257138	Apr 26, 2021 (155)
13	GNOMAD	ss4065257139	Apr 26, 2021 (155)
14	GNOMAD	ss4065257140	Apr 26, 2021 (155)
15	GNOMAD	ss4065257141	Apr 26, 2021 (155)
16	GNOMAD	ss4065257142	Apr 26, 2021 (155)
17	GNOMAD	ss4065257143	Apr 26, 2021 (155)
18	GNOMAD	ss4065257144	Apr 26, 2021 (155)
19	GNOMAD	ss4065257145	Apr 26, 2021 (155)
20	GNOMAD	ss4065257146	Apr 26, 2021 (155)
21	GNOMAD	ss4065257147	Apr 26, 2021 (155)
22	GNOMAD	ss4065257148	Apr 26, 2021 (155)
23	TOMMO_GENOMICS	ss5688859174	Oct 12, 2022 (156)
24	TOMMO_GENOMICS	ss5688859175	Oct 12, 2022 (156)
25	TOMMO_GENOMICS	ss5688859176	Oct 12, 2022 (156)
26	TOMMO_GENOMICS	ss5688859177	Oct 12, 2022 (156)
27	EVA	ss5853473962	Oct 12, 2022 (156)
28	gnomAD - Genomes Submission ignored due to conflicting rows: Row 98023543 (NC_000003.12:6715692::T 6308/109328) Row 98023624 (NC_000003.12:6715692::TT 1033/109394) Row 98023625 (NC_000003.12:6715692::TTT 418/109402)...	-	Apr 26, 2021 (155)
29	gnomAD - Genomes Submission ignored due to conflicting rows: Row 98023543 (NC_000003.12:6715692::T 6308/109328) Row 98023624 (NC_000003.12:6715692::TT 1033/109394) Row 98023625 (NC_000003.12:6715692::TTT 418/109402)...	-	Apr 26, 2021 (155)
30	gnomAD - Genomes Submission ignored due to conflicting rows: Row 98023543 (NC_000003.12:6715692::T 6308/109328) Row 98023624 (NC_000003.12:6715692::TT 1033/109394) Row 98023625 (NC_000003.12:6715692::TTT 418/109402)...	-	Apr 26, 2021 (155)
31	gnomAD - Genomes Submission ignored due to conflicting rows: Row 98023543 (NC_000003.12:6715692::T 6308/109328) Row 98023624 (NC_000003.12:6715692::TT 1033/109394) Row 98023625 (NC_000003.12:6715692::TTT 418/109402)...	-	Apr 26, 2021 (155)
32	gnomAD - Genomes Submission ignored due to conflicting rows: Row 98023543 (NC_000003.12:6715692::T 6308/109328) Row 98023624 (NC_000003.12:6715692::TT 1033/109394) Row 98023625 (NC_000003.12:6715692::TTT 418/109402)...	-	Apr 26, 2021 (155)
33	gnomAD - Genomes Submission ignored due to conflicting rows: Row 98023543 (NC_000003.12:6715692::T 6308/109328) Row 98023624 (NC_000003.12:6715692::TT 1033/109394) Row 98023625 (NC_000003.12:6715692::TTT 418/109402)...	-	Apr 26, 2021 (155)
34	gnomAD - Genomes Submission ignored due to conflicting rows: Row 98023543 (NC_000003.12:6715692::T 6308/109328) Row 98023624 (NC_000003.12:6715692::TT 1033/109394) Row 98023625 (NC_000003.12:6715692::TTT 418/109402)...	-	Apr 26, 2021 (155)
35	gnomAD - Genomes Submission ignored due to conflicting rows: Row 98023543 (NC_000003.12:6715692::T 6308/109328) Row 98023624 (NC_000003.12:6715692::TT 1033/109394) Row 98023625 (NC_000003.12:6715692::TTT 418/109402)...	-	Apr 26, 2021 (155)
36	gnomAD - Genomes Submission ignored due to conflicting rows: Row 98023543 (NC_000003.12:6715692::T 6308/109328) Row 98023624 (NC_000003.12:6715692::TT 1033/109394) Row 98023625 (NC_000003.12:6715692::TTT 418/109402)...	-	Apr 26, 2021 (155)
37	gnomAD - Genomes Submission ignored due to conflicting rows: Row 98023543 (NC_000003.12:6715692::T 6308/109328) Row 98023624 (NC_000003.12:6715692::TT 1033/109394) Row 98023625 (NC_000003.12:6715692::TTT 418/109402)...	-	Apr 26, 2021 (155)
38	gnomAD - Genomes Submission ignored due to conflicting rows: Row 98023543 (NC_000003.12:6715692::T 6308/109328) Row 98023624 (NC_000003.12:6715692::TT 1033/109394) Row 98023625 (NC_000003.12:6715692::TTT 418/109402)...	-	Apr 26, 2021 (155)
39	gnomAD - Genomes Submission ignored due to conflicting rows: Row 98023543 (NC_000003.12:6715692::T 6308/109328) Row 98023624 (NC_000003.12:6715692::TT 1033/109394) Row 98023625 (NC_000003.12:6715692::TTT 418/109402)...	-	Apr 26, 2021 (155)
40	gnomAD - Genomes Submission ignored due to conflicting rows: Row 98023543 (NC_000003.12:6715692::T 6308/109328) Row 98023624 (NC_000003.12:6715692::TT 1033/109394) Row 98023625 (NC_000003.12:6715692::TTT 418/109402)...	-	Apr 26, 2021 (155)
41	gnomAD - Genomes Submission ignored due to conflicting rows: Row 98023543 (NC_000003.12:6715692::T 6308/109328) Row 98023624 (NC_000003.12:6715692::TT 1033/109394) Row 98023625 (NC_000003.12:6715692::TTT 418/109402)...	-	Apr 26, 2021 (155)
42	gnomAD - Genomes Submission ignored due to conflicting rows: Row 98023543 (NC_000003.12:6715692::T 6308/109328) Row 98023624 (NC_000003.12:6715692::TT 1033/109394) Row 98023625 (NC_000003.12:6715692::TTT 418/109402)...	-	Apr 26, 2021 (155)
43	Korean Genome Project Submission ignored due to conflicting rows: Row 6970775 (NC_000003.12:6715692:T: 296/1788) Row 6970776 (NC_000003.12:6715693::TT 4/1788) Row 6970777 (NC_000003.12:6715693::T 91/1788)	-	Apr 25, 2020 (154)
44	Korean Genome Project Submission ignored due to conflicting rows: Row 6970775 (NC_000003.12:6715692:T: 296/1788) Row 6970776 (NC_000003.12:6715693::TT 4/1788) Row 6970777 (NC_000003.12:6715693::T 91/1788)	-	Apr 25, 2020 (154)
45	Korean Genome Project Submission ignored due to conflicting rows: Row 6970775 (NC_000003.12:6715692:T: 296/1788) Row 6970776 (NC_000003.12:6715693::TT 4/1788) Row 6970777 (NC_000003.12:6715693::T 91/1788)	-	Apr 25, 2020 (154)
46	Northern Sweden	NC_000003.11 - 6757380	Jul 13, 2019 (153)
47	14KJPN Submission ignored due to conflicting rows: Row 22696278 (NC_000003.12:6715692::TT 27/28230) Row 22696279 (NC_000003.12:6715692:T: 3877/28230) Row 22696280 (NC_000003.12:6715692::T 2169/28230)...	-	Oct 12, 2022 (156)
48	14KJPN Submission ignored due to conflicting rows: Row 22696278 (NC_000003.12:6715692::TT 27/28230) Row 22696279 (NC_000003.12:6715692:T: 3877/28230) Row 22696280 (NC_000003.12:6715692::T 2169/28230)...	-	Oct 12, 2022 (156)
49	14KJPN Submission ignored due to conflicting rows: Row 22696278 (NC_000003.12:6715692::TT 27/28230) Row 22696279 (NC_000003.12:6715692:T: 3877/28230) Row 22696280 (NC_000003.12:6715692::T 2169/28230)...	-	Oct 12, 2022 (156)
50	14KJPN Submission ignored due to conflicting rows: Row 22696278 (NC_000003.12:6715692::TT 27/28230) Row 22696279 (NC_000003.12:6715692:T: 3877/28230) Row 22696280 (NC_000003.12:6715692::T 2169/28230)...	-	Oct 12, 2022 (156)
51	ALFA	NC_000003.12 - 6715693	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
228669685	NC_000003.12:6715692:TTTTTTTTTTTTT… NC_000003.12:6715692:TTTTTTTTTTTTTT:TTTTTTTTT	NC_000003.12:6715692:TTTTTTTTTTTTT… NC_000003.12:6715692:TTTTTTTTTTTTTT:TTTTTTTTT	(self)
228669685	NC_000003.12:6715692:TTTTTTTTTTTTT… NC_000003.12:6715692:TTTTTTTTTTTTTT:TTTTTTTTTT	NC_000003.12:6715692:TTTTTTTTTTTTT… NC_000003.12:6715692:TTTTTTTTTTTTTT:TTTTTTTTTT	(self)
ss4065257148	NC_000003.12:6715692:TTT:	NC_000003.12:6715692:TTTTTTTTTTTTT… NC_000003.12:6715692:TTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
228669685	NC_000003.12:6715692:TTTTTTTTTTTTT… NC_000003.12:6715692:TTTTTTTTTTTTTT:TTTTTTTTTTT	NC_000003.12:6715692:TTTTTTTTTTTTT… NC_000003.12:6715692:TTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss4065257147, ss5688859177	NC_000003.12:6715692:TT:	NC_000003.12:6715692:TTTTTTTTTTTTT… NC_000003.12:6715692:TTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
228669685	NC_000003.12:6715692:TTTTTTTTTTTTT… NC_000003.12:6715692:TTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000003.12:6715692:TTTTTTTTTTTTT… NC_000003.12:6715692:TTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss663422391	NC_000003.11:6757379:T:	NC_000003.12:6715692:TTTTTTTTTTTTT… NC_000003.12:6715692:TTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss3950592774, ss4065257146, ss5688859175, ss5853473962	NC_000003.12:6715692:T:	NC_000003.12:6715692:TTTTTTTTTTTTT… NC_000003.12:6715692:TTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
228669685	NC_000003.12:6715692:TTTTTTTTTTTTT… NC_000003.12:6715692:TTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000003.12:6715692:TTTTTTTTTTTTT… NC_000003.12:6715692:TTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
2884950, ss3729600085	NC_000003.11:6757379::T	NC_000003.12:6715692:TTTTTTTTTTTTT… NC_000003.12:6715692:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3708565117, ss4065257054, ss5688859176	NC_000003.12:6715692::T	NC_000003.12:6715692:TTTTTTTTTTTTT… NC_000003.12:6715692:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
228669685	NC_000003.12:6715692:TTTTTTTTTTTTT… NC_000003.12:6715692:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000003.12:6715692:TTTTTTTTTTTTT… NC_000003.12:6715692:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3950592776	NC_000003.12:6715693::T	NC_000003.12:6715692:TTTTTTTTTTTTT… NC_000003.12:6715692:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4065257135, ss5688859174	NC_000003.12:6715692::TT	NC_000003.12:6715692:TTTTTTTTTTTTT… NC_000003.12:6715692:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
228669685	NC_000003.12:6715692:TTTTTTTTTTTTT… NC_000003.12:6715692:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000003.12:6715692:TTTTTTTTTTTTT… NC_000003.12:6715692:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3950592775	NC_000003.12:6715693::TT	NC_000003.12:6715692:TTTTTTTTTTTTT… NC_000003.12:6715692:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4065257136	NC_000003.12:6715692::TTT	NC_000003.12:6715692:TTTTTTTTTTTTT… NC_000003.12:6715692:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
228669685	NC_000003.12:6715692:TTTTTTTTTTTTT… NC_000003.12:6715692:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000003.12:6715692:TTTTTTTTTTTTT… NC_000003.12:6715692:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4065257137	NC_000003.12:6715692::TTTT	NC_000003.12:6715692:TTTTTTTTTTTTT… NC_000003.12:6715692:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
228669685	NC_000003.12:6715692:TTTTTTTTTTTTT… NC_000003.12:6715692:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000003.12:6715692:TTTTTTTTTTTTT… NC_000003.12:6715692:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4065257138	NC_000003.12:6715692::TTTTT	NC_000003.12:6715692:TTTTTTTTTTTTT… NC_000003.12:6715692:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
228669685	NC_000003.12:6715692:TTTTTTTTTTTTT… NC_000003.12:6715692:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000003.12:6715692:TTTTTTTTTTTTT… NC_000003.12:6715692:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4065257139	NC_000003.12:6715692::TTTTTT	NC_000003.12:6715692:TTTTTTTTTTTTT… NC_000003.12:6715692:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
228669685	NC_000003.12:6715692:TTTTTTTTTTTTT… NC_000003.12:6715692:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000003.12:6715692:TTTTTTTTTTTTT… NC_000003.12:6715692:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4065257140	NC_000003.12:6715692::TTTTTTT	NC_000003.12:6715692:TTTTTTTTTTTTT… NC_000003.12:6715692:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss3708565118, ss4065257141	NC_000003.12:6715692::TTTTTTTT	NC_000003.12:6715692:TTTTTTTTTTTTT… NC_000003.12:6715692:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4065257142	NC_000003.12:6715692::TTTTTTTTT	NC_000003.12:6715692:TTTTTTTTTTTTT… NC_000003.12:6715692:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4065257143	NC_000003.12:6715692::TTTTTTTTTT	NC_000003.12:6715692:TTTTTTTTTTTTT… NC_000003.12:6715692:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4065257144	NC_000003.12:6715692::TTTTTTTTTTT	NC_000003.12:6715692:TTTTTTTTTTTTT… NC_000003.12:6715692:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
228669685	NC_000003.12:6715692:TTTTTTTTTTTTT… NC_000003.12:6715692:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000003.12:6715692:TTTTTTTTTTTTT… NC_000003.12:6715692:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4065257145	NC_000003.12:6715692::TTTTTTTTTTTTT	NC_000003.12:6715692:TTTTTTTTTTTTT… NC_000003.12:6715692:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(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 rs764981282

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

rs764981282