Name: rs34133897
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.

rs34133897

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr15:43619922-43619938 (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: delTT / delT / dupT / dupTT / dupT…
delTT / delT / dupT / dupTT / dupTTT / dup(T)₈
Variation Type: Indel Insertion and Deletion
Frequency: delTT=0.00000 (0/11490, ALFA)
delT=0.00000 (0/11490, ALFA)
dupT=0.00000 (0/11490, ALFA) (+ 1 more)
dupTT=0.00000 (0/11490, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: STRC : 2KB Upstream 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	11490	TTTTTTTTTTTTTTTTT=1.00000	TTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTT=0.00000	1.0	N/A
European	Sub	7488	TTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
African	Sub	2784	TTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
African Others	Sub	108	TTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000	1.0	N/A
African American	Sub	2676	TTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
Asian	Sub	56	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
East Asian	Sub	44	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Other Asian	Sub	12	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Latin American 1	Sub	142	TTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000	1.0	N/A
Latin American 2	Sub	496	TTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000	1.0	N/A
South Asian	Sub	88	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Other	Sub	436	TTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000	1.0	N/A

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

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	11490	(T)₁₇=1.00000	delTT=0.00000, delT=0.00000, dupT=0.00000, dupTT=0.00000
Allele Frequency Aggregator	European	Sub	7488	(T)₁₇=1.0000	delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000
Allele Frequency Aggregator	African	Sub	2784	(T)₁₇=1.0000	delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	496	(T)₁₇=1.000	delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000
Allele Frequency Aggregator	Other	Sub	436	(T)₁₇=1.000	delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000
Allele Frequency Aggregator	Latin American 1	Sub	142	(T)₁₇=1.000	delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000
Allele Frequency Aggregator	South Asian	Sub	88	(T)₁₇=1.00	delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00
Allele Frequency Aggregator	Asian	Sub	56	(T)₁₇=1.00	delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00

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

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 15	NC_000015.10:g.43619937_43619938del
GRCh38.p14 chr 15	NC_000015.10:g.43619938del
GRCh38.p14 chr 15	NC_000015.10:g.43619938dup
GRCh38.p14 chr 15	NC_000015.10:g.43619937_43619938dup
GRCh38.p14 chr 15	NC_000015.10:g.43619936_43619938dup
GRCh38.p14 chr 15	NC_000015.10:g.43619931_43619938dup
GRCh37.p13 chr 15	NC_000015.9:g.43912135_43912136del
GRCh37.p13 chr 15	NC_000015.9:g.43912136del
GRCh37.p13 chr 15	NC_000015.9:g.43912136dup
GRCh37.p13 chr 15	NC_000015.9:g.43912135_43912136dup
GRCh37.p13 chr 15	NC_000015.9:g.43912134_43912136dup
GRCh37.p13 chr 15	NC_000015.9:g.43912129_43912136dup
STRC RefSeqGene	NG_011636.1:g.3878_3879del
STRC RefSeqGene	NG_011636.1:g.3879del
STRC RefSeqGene	NG_011636.1:g.3879dup
STRC RefSeqGene	NG_011636.1:g.3878_3879dup
STRC RefSeqGene	NG_011636.1:g.3877_3879dup
STRC RefSeqGene	NG_011636.1:g.3872_3879dup

Gene: STRC, stereocilin (minus strand) : 2KB Upstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
STRC transcript	NM_153700.2:c.	N/A	Upstream 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)₁₇=	delTT	delT	dupT	dupTT	dupTTT	dup(T)₈
GRCh38.p14 chr 15	NC_000015.10:g.43619922_43619938=	NC_000015.10:g.43619937_43619938del	NC_000015.10:g.43619938del	NC_000015.10:g.43619938dup	NC_000015.10:g.43619937_43619938dup	NC_000015.10:g.43619936_43619938dup	NC_000015.10:g.43619931_43619938dup
GRCh37.p13 chr 15	NC_000015.9:g.43912120_43912136=	NC_000015.9:g.43912135_43912136del	NC_000015.9:g.43912136del	NC_000015.9:g.43912136dup	NC_000015.9:g.43912135_43912136dup	NC_000015.9:g.43912134_43912136dup	NC_000015.9:g.43912129_43912136dup
STRC RefSeqGene	NG_011636.1:g.3863_3879=	NG_011636.1:g.3878_3879del	NG_011636.1:g.3879del	NG_011636.1:g.3879dup	NG_011636.1:g.3878_3879dup	NG_011636.1:g.3877_3879dup	NG_011636.1:g.3872_3879dup
STRC transcript variant X1	XM_005254193.1:c.-48-1152=	XM_005254193.1:c.-48-1153_-48-1152del	XM_005254193.1:c.-48-1152del	XM_005254193.1:c.-48-1152dup	XM_005254193.1:c.-48-1153_-48-1152dup	XM_005254193.1:c.-48-1154_-48-1152dup	XM_005254193.1:c.-48-1159_-48-1152dup

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#.

25 SubSNP, 18 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss40589088	Dec 03, 2013 (138)
2	ABI	ss40617220	Mar 13, 2006 (126)
3	PJP	ss294857212	May 09, 2011 (142)
4	URBANLAB	ss3650342231	Oct 12, 2018 (152)
5	KOGIC	ss3976028206	Apr 27, 2020 (154)
6	KOGIC	ss3976028207	Apr 27, 2020 (154)
7	KOGIC	ss3976028208	Apr 27, 2020 (154)
8	GNOMAD	ss4287762761	Apr 27, 2021 (155)
9	GNOMAD	ss4287762762	Apr 27, 2021 (155)
10	GNOMAD	ss4287762763	Apr 27, 2021 (155)
11	GNOMAD	ss4287762764	Apr 27, 2021 (155)
12	GNOMAD	ss4287762766	Apr 27, 2021 (155)
13	TOMMO_GENOMICS	ss5215924476	Apr 27, 2021 (155)
14	TOMMO_GENOMICS	ss5215924477	Apr 27, 2021 (155)
15	TOMMO_GENOMICS	ss5215924478	Apr 27, 2021 (155)
16	TOMMO_GENOMICS	ss5215924479	Apr 27, 2021 (155)
17	1000G_HIGH_COVERAGE	ss5298242446	Oct 16, 2022 (156)
18	1000G_HIGH_COVERAGE	ss5298242447	Oct 16, 2022 (156)
19	1000G_HIGH_COVERAGE	ss5298242448	Oct 16, 2022 (156)
20	HUGCELL_USP	ss5491993974	Oct 16, 2022 (156)
21	HUGCELL_USP	ss5491993975	Oct 16, 2022 (156)
22	TOMMO_GENOMICS	ss5769651006	Oct 16, 2022 (156)
23	TOMMO_GENOMICS	ss5769651008	Oct 16, 2022 (156)
24	TOMMO_GENOMICS	ss5769651009	Oct 16, 2022 (156)
25	TOMMO_GENOMICS	ss5769651010	Oct 16, 2022 (156)
26	gnomAD - Genomes Submission ignored due to conflicting rows: Row 467370179 (NC_000015.10:43619921::T 2106/77238) Row 467370180 (NC_000015.10:43619921::TT 10/77282) Row 467370181 (NC_000015.10:43619921::TTT 3/77282)...	-	Apr 27, 2021 (155)
27	gnomAD - Genomes Submission ignored due to conflicting rows: Row 467370179 (NC_000015.10:43619921::T 2106/77238) Row 467370180 (NC_000015.10:43619921::TT 10/77282) Row 467370181 (NC_000015.10:43619921::TTT 3/77282)...	-	Apr 27, 2021 (155)
28	gnomAD - Genomes Submission ignored due to conflicting rows: Row 467370179 (NC_000015.10:43619921::T 2106/77238) Row 467370180 (NC_000015.10:43619921::TT 10/77282) Row 467370181 (NC_000015.10:43619921::TTT 3/77282)...	-	Apr 27, 2021 (155)
29	gnomAD - Genomes Submission ignored due to conflicting rows: Row 467370179 (NC_000015.10:43619921::T 2106/77238) Row 467370180 (NC_000015.10:43619921::TT 10/77282) Row 467370181 (NC_000015.10:43619921::TTT 3/77282)...	-	Apr 27, 2021 (155)
30	gnomAD - Genomes Submission ignored due to conflicting rows: Row 467370179 (NC_000015.10:43619921::T 2106/77238) Row 467370180 (NC_000015.10:43619921::TT 10/77282) Row 467370181 (NC_000015.10:43619921::TTT 3/77282)...	-	Apr 27, 2021 (155)
31	gnomAD - Genomes Submission ignored due to conflicting rows: Row 467370179 (NC_000015.10:43619921::T 2106/77238) Row 467370180 (NC_000015.10:43619921::TT 10/77282) Row 467370181 (NC_000015.10:43619921::TTT 3/77282)...	-	Apr 27, 2021 (155)
32	Korean Genome Project Submission ignored due to conflicting rows: Row 32406207 (NC_000015.10:43619924:T: 155/1822) Row 32406208 (NC_000015.10:43619925::T 339/1822) Row 32406209 (NC_000015.10:43619923:TT: 69/1822)	-	Apr 27, 2020 (154)
33	Korean Genome Project Submission ignored due to conflicting rows: Row 32406207 (NC_000015.10:43619924:T: 155/1822) Row 32406208 (NC_000015.10:43619925::T 339/1822) Row 32406209 (NC_000015.10:43619923:TT: 69/1822)	-	Apr 27, 2020 (154)
34	Korean Genome Project Submission ignored due to conflicting rows: Row 32406207 (NC_000015.10:43619924:T: 155/1822) Row 32406208 (NC_000015.10:43619925::T 339/1822) Row 32406209 (NC_000015.10:43619923:TT: 69/1822)	-	Apr 27, 2020 (154)
35	8.3KJPN Submission ignored due to conflicting rows: Row 73893783 (NC_000015.9:43912119:T: 692/16466) Row 73893784 (NC_000015.9:43912119::T 3137/16466) Row 73893785 (NC_000015.9:43912119:TT: 379/16466)...	-	Apr 27, 2021 (155)
36	8.3KJPN Submission ignored due to conflicting rows: Row 73893783 (NC_000015.9:43912119:T: 692/16466) Row 73893784 (NC_000015.9:43912119::T 3137/16466) Row 73893785 (NC_000015.9:43912119:TT: 379/16466)...	-	Apr 27, 2021 (155)
37	8.3KJPN Submission ignored due to conflicting rows: Row 73893783 (NC_000015.9:43912119:T: 692/16466) Row 73893784 (NC_000015.9:43912119::T 3137/16466) Row 73893785 (NC_000015.9:43912119:TT: 379/16466)...	-	Apr 27, 2021 (155)
38	8.3KJPN Submission ignored due to conflicting rows: Row 73893783 (NC_000015.9:43912119:T: 692/16466) Row 73893784 (NC_000015.9:43912119::T 3137/16466) Row 73893785 (NC_000015.9:43912119:TT: 379/16466)...	-	Apr 27, 2021 (155)
39	14KJPN Submission ignored due to conflicting rows: Row 103488110 (NC_000015.10:43619921:TT: 748/27456) Row 103488112 (NC_000015.10:43619921::T 5275/27456) Row 103488113 (NC_000015.10:43619921:T: 1252/27456)...	-	Oct 16, 2022 (156)
40	14KJPN Submission ignored due to conflicting rows: Row 103488110 (NC_000015.10:43619921:TT: 748/27456) Row 103488112 (NC_000015.10:43619921::T 5275/27456) Row 103488113 (NC_000015.10:43619921:T: 1252/27456)...	-	Oct 16, 2022 (156)
41	14KJPN Submission ignored due to conflicting rows: Row 103488110 (NC_000015.10:43619921:TT: 748/27456) Row 103488112 (NC_000015.10:43619921::T 5275/27456) Row 103488113 (NC_000015.10:43619921:T: 1252/27456)...	-	Oct 16, 2022 (156)
42	14KJPN Submission ignored due to conflicting rows: Row 103488110 (NC_000015.10:43619921:TT: 748/27456) Row 103488112 (NC_000015.10:43619921::T 5275/27456) Row 103488113 (NC_000015.10:43619921:T: 1252/27456)...	-	Oct 16, 2022 (156)
43	ALFA	NC_000015.10 - 43619922	Apr 27, 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)
rs34300937	Aug 21, 2014 (142)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss5215924478	NC_000015.9:43912119:TT:	NC_000015.10:43619921:TTTTTTTTTTTT… NC_000015.10:43619921:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4287762766, ss5298242448, ss5769651006	NC_000015.10:43619921:TT:	NC_000015.10:43619921:TTTTTTTTTTTT… NC_000015.10:43619921:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
2525926975	NC_000015.10:43619921:TTTTTTTTTTTT… NC_000015.10:43619921:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000015.10:43619921:TTTTTTTTTTTT… NC_000015.10:43619921:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3976028208	NC_000015.10:43619923:TT:	NC_000015.10:43619921:TTTTTTTTTTTT… NC_000015.10:43619921:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss5215924476	NC_000015.9:43912119:T:	NC_000015.10:43619921:TTTTTTTTTTTT… NC_000015.10:43619921:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3650342231, ss5298242447, ss5491993975, ss5769651009	NC_000015.10:43619921:T:	NC_000015.10:43619921:TTTTTTTTTTTT… NC_000015.10:43619921:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
2525926975	NC_000015.10:43619921:TTTTTTTTTTTT… NC_000015.10:43619921:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000015.10:43619921:TTTTTTTTTTTT… NC_000015.10:43619921:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3976028206	NC_000015.10:43619924:T:	NC_000015.10:43619921:TTTTTTTTTTTT… NC_000015.10:43619921:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss40589088	NT_010194.17:14702692:T:	NC_000015.10:43619921:TTTTTTTTTTTT… NC_000015.10:43619921:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss294857212	NC_000015.8:41699428::T	NC_000015.10:43619921:TTTTTTTTTTTT… NC_000015.10:43619921:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss5215924477	NC_000015.9:43912119::T	NC_000015.10:43619921:TTTTTTTTTTTT… NC_000015.10:43619921:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4287762761, ss5298242446, ss5491993974, ss5769651008	NC_000015.10:43619921::T	NC_000015.10:43619921:TTTTTTTTTTTT… NC_000015.10:43619921:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
2525926975	NC_000015.10:43619921:TTTTTTTTTTTT… NC_000015.10:43619921:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000015.10:43619921:TTTTTTTTTTTT… NC_000015.10:43619921:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3976028207	NC_000015.10:43619925::T	NC_000015.10:43619921:TTTTTTTTTTTT… NC_000015.10:43619921:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss40617220	NT_010194.17:14702693::T	NC_000015.10:43619921:TTTTTTTTTTTT… NC_000015.10:43619921:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss5215924479	NC_000015.9:43912119::TT	NC_000015.10:43619921:TTTTTTTTTTTT… NC_000015.10:43619921:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4287762762, ss5769651010	NC_000015.10:43619921::TT	NC_000015.10:43619921:TTTTTTTTTTTT… NC_000015.10:43619921:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
2525926975	NC_000015.10:43619921:TTTTTTTTTTTT… NC_000015.10:43619921:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000015.10:43619921:TTTTTTTTTTTT… NC_000015.10:43619921:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4287762763	NC_000015.10:43619921::TTT	NC_000015.10:43619921:TTTTTTTTTTTT… NC_000015.10:43619921:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4287762764	NC_000015.10:43619921::TTTTTTTT	NC_000015.10:43619921:TTTTTTTTTTTT… NC_000015.10:43619921:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(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 rs34133897

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

rs34133897