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dbSNP Short Genetic Variations

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.

rs34151345

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr1:111908952-111908967 (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)4

Variation Type
Indel Insertion and Deletion
Frequency
dupT=0.1819 (1251/6876, ALFA)
dupT=0.4046 (2026/5008, 1000G)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
KCND3 : Intron Variant
KCND3-AS1 : 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 Alt HMOZ HTRZ HWEP
Total Global 6876 TTTTTTTTTTTTTTTT=0.7586 TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0004, TTTTTTTTTTTTTTTTT=0.1819, TTTTTTTTTTTTTTTTTTT=0.0048, TTTTTTTTTTTTTTTTTT=0.0542, TTTTTTTTTTTTTTTTTTTT=0.0000 0.744148 0.104681 0.15117 32
European Sub 6082 TTTTTTTTTTTTTTTT=0.7279 TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0005, TTTTTTTTTTTTTTTTT=0.2050, TTTTTTTTTTTTTTTTTTT=0.0054, TTTTTTTTTTTTTTTTTT=0.0612, TTTTTTTTTTTTTTTTTTTT=0.0000 0.707463 0.119776 0.172761 32
African Sub 488 TTTTTTTTTTTTTTTT=1.000 TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000 1.0 0.0 0.0 N/A
African Others Sub 16 TTTTTTTTTTTTTTTT=1.00 TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00 1.0 0.0 0.0 N/A
African American Sub 472 TTTTTTTTTTTTTTTT=1.000 TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000 1.0 0.0 0.0 N/A
Asian Sub 18 TTTTTTTTTTTTTTTT=1.00 TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00 1.0 0.0 0.0 N/A
East Asian Sub 14 TTTTTTTTTTTTTTTT=1.00 TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00 1.0 0.0 0.0 N/A
Other Asian Sub 4 TTTTTTTTTTTTTTTT=1.0 TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0 1.0 0.0 0.0 N/A
Latin American 1 Sub 40 TTTTTTTTTTTTTTTT=1.00 TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00 1.0 0.0 0.0 N/A
Latin American 2 Sub 128 TTTTTTTTTTTTTTTT=1.000 TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000 1.0 0.0 0.0 N/A
South Asian Sub 22 TTTTTTTTTTTTTTTT=1.00 TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00 1.0 0.0 0.0 N/A
Other Sub 98 TTTTTTTTTTTTTTTT=0.95 TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.04, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.01, TTTTTTTTTTTTTTTTTTTT=0.00 0.9375 0.020833 0.041667 6


Help

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 6876 (T)16=0.7586 delTT=0.0000, delT=0.0004, dupT=0.1819, dupTT=0.0542, dupTTT=0.0048, dup(T)4=0.0000
Allele Frequency Aggregator European Sub 6082 (T)16=0.7279 delTT=0.0000, delT=0.0005, dupT=0.2050, dupTT=0.0612, dupTTT=0.0054, dup(T)4=0.0000
Allele Frequency Aggregator African Sub 488 (T)16=1.000 delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)4=0.000
Allele Frequency Aggregator Latin American 2 Sub 128 (T)16=1.000 delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)4=0.000
Allele Frequency Aggregator Other Sub 98 (T)16=0.95 delTT=0.00, delT=0.00, dupT=0.04, dupTT=0.01, dupTTT=0.00, dup(T)4=0.00
Allele Frequency Aggregator Latin American 1 Sub 40 (T)16=1.00 delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)4=0.00
Allele Frequency Aggregator South Asian Sub 22 (T)16=1.00 delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)4=0.00
Allele Frequency Aggregator Asian Sub 18 (T)16=1.00 delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)4=0.00
1000Genomes Global Study-wide 5008 -

No frequency provided

dupT=0.4046
1000Genomes African Sub 1322 -

No frequency provided

dupT=0.4894
1000Genomes East Asian Sub 1008 -

No frequency provided

dupT=0.3710
1000Genomes Europe Sub 1006 -

No frequency provided

dupT=0.3499
1000Genomes South Asian Sub 978 -

No frequency provided

dupT=0.398
1000Genomes American Sub 694 -

No frequency provided

dupT=0.380
Help

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 1 NC_000001.11:g.111908966_111908967del
GRCh38.p14 chr 1 NC_000001.11:g.111908967del
GRCh38.p14 chr 1 NC_000001.11:g.111908967dup
GRCh38.p14 chr 1 NC_000001.11:g.111908966_111908967dup
GRCh38.p14 chr 1 NC_000001.11:g.111908965_111908967dup
GRCh38.p14 chr 1 NC_000001.11:g.111908964_111908967dup
GRCh37.p13 chr 1 NC_000001.10:g.112451588_112451589del
GRCh37.p13 chr 1 NC_000001.10:g.112451589del
GRCh37.p13 chr 1 NC_000001.10:g.112451589dup
GRCh37.p13 chr 1 NC_000001.10:g.112451588_112451589dup
GRCh37.p13 chr 1 NC_000001.10:g.112451587_112451589dup
GRCh37.p13 chr 1 NC_000001.10:g.112451586_112451589dup
KCND3 RefSeqGene (LRG_445) NG_032011.2:g.85203_85204del
KCND3 RefSeqGene (LRG_445) NG_032011.2:g.85204del
KCND3 RefSeqGene (LRG_445) NG_032011.2:g.85204dup
KCND3 RefSeqGene (LRG_445) NG_032011.2:g.85203_85204dup
KCND3 RefSeqGene (LRG_445) NG_032011.2:g.85202_85204dup
KCND3 RefSeqGene (LRG_445) NG_032011.2:g.85201_85204dup
Gene: KCND3, potassium voltage-gated channel subfamily D member 3 (minus strand)
Molecule type Change Amino acid[Codon] SO Term
KCND3 transcript variant 3 NM_001378969.1:c.1106+726…

NM_001378969.1:c.1106+72668_1106+72669del

N/A Intron Variant
KCND3 transcript variant 4 NM_001378970.1:c.1106+726…

NM_001378970.1:c.1106+72668_1106+72669del

N/A Intron Variant
KCND3 transcript variant 1 NM_004980.5:c.1106+72668_…

NM_004980.5:c.1106+72668_1106+72669del

N/A Intron Variant
KCND3 transcript variant 2 NM_172198.3:c.1106+72668_…

NM_172198.3:c.1106+72668_1106+72669del

N/A Intron Variant
KCND3 transcript variant X1 XM_006710629.5:c.1106+726…

XM_006710629.5:c.1106+72668_1106+72669del

N/A Intron Variant
KCND3 transcript variant X6 XM_006710632.4:c.1107-129…

XM_006710632.4:c.1107-12962_1107-12961del

N/A Intron Variant
KCND3 transcript variant X7 XM_011541427.4:c.1106+726…

XM_011541427.4:c.1106+72668_1106+72669del

N/A Intron Variant
KCND3 transcript variant X2 XM_017001244.3:c.1106+726…

XM_017001244.3:c.1106+72668_1106+72669del

N/A Intron Variant
KCND3 transcript variant X3 XM_011541425.4:c. N/A Genic Downstream Transcript Variant
KCND3 transcript variant X5 XM_011541426.3:c. N/A Genic Downstream Transcript Variant
KCND3 transcript variant X8 XM_011541428.3:c. N/A Genic Downstream Transcript Variant
KCND3 transcript variant X4 XM_017001245.3:c. N/A Genic Downstream Transcript Variant
Gene: KCND3-AS1, KCND3 antisense RNA 1 (plus strand) : 2KB Upstream Variant
Molecule type Change Amino acid[Codon] SO Term
KCND3-AS1 transcript NR_046619.1:n. N/A Upstream Transcript Variant
Help

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
Help

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)16= delTT delT dupT dupTT dupTTT dup(T)4
GRCh38.p14 chr 1 NC_000001.11:g.111908952_111908967= NC_000001.11:g.111908966_111908967del NC_000001.11:g.111908967del NC_000001.11:g.111908967dup NC_000001.11:g.111908966_111908967dup NC_000001.11:g.111908965_111908967dup NC_000001.11:g.111908964_111908967dup
GRCh37.p13 chr 1 NC_000001.10:g.112451574_112451589= NC_000001.10:g.112451588_112451589del NC_000001.10:g.112451589del NC_000001.10:g.112451589dup NC_000001.10:g.112451588_112451589dup NC_000001.10:g.112451587_112451589dup NC_000001.10:g.112451586_112451589dup
KCND3 RefSeqGene (LRG_445) NG_032011.2:g.85189_85204= NG_032011.2:g.85203_85204del NG_032011.2:g.85204del NG_032011.2:g.85204dup NG_032011.2:g.85203_85204dup NG_032011.2:g.85202_85204dup NG_032011.2:g.85201_85204dup
KCND3 transcript variant 3 NM_001378969.1:c.1106+72669= NM_001378969.1:c.1106+72668_1106+72669del NM_001378969.1:c.1106+72669del NM_001378969.1:c.1106+72669dup NM_001378969.1:c.1106+72668_1106+72669dup NM_001378969.1:c.1106+72667_1106+72669dup NM_001378969.1:c.1106+72666_1106+72669dup
KCND3 transcript variant 4 NM_001378970.1:c.1106+72669= NM_001378970.1:c.1106+72668_1106+72669del NM_001378970.1:c.1106+72669del NM_001378970.1:c.1106+72669dup NM_001378970.1:c.1106+72668_1106+72669dup NM_001378970.1:c.1106+72667_1106+72669dup NM_001378970.1:c.1106+72666_1106+72669dup
KCND3 transcript variant 1 NM_004980.4:c.1106+72669= NM_004980.4:c.1106+72668_1106+72669del NM_004980.4:c.1106+72669del NM_004980.4:c.1106+72669dup NM_004980.4:c.1106+72668_1106+72669dup NM_004980.4:c.1106+72667_1106+72669dup NM_004980.4:c.1106+72666_1106+72669dup
KCND3 transcript variant 1 NM_004980.5:c.1106+72669= NM_004980.5:c.1106+72668_1106+72669del NM_004980.5:c.1106+72669del NM_004980.5:c.1106+72669dup NM_004980.5:c.1106+72668_1106+72669dup NM_004980.5:c.1106+72667_1106+72669dup NM_004980.5:c.1106+72666_1106+72669dup
KCND3 transcript variant 2 NM_172198.2:c.1106+72669= NM_172198.2:c.1106+72668_1106+72669del NM_172198.2:c.1106+72669del NM_172198.2:c.1106+72669dup NM_172198.2:c.1106+72668_1106+72669dup NM_172198.2:c.1106+72667_1106+72669dup NM_172198.2:c.1106+72666_1106+72669dup
KCND3 transcript variant 2 NM_172198.3:c.1106+72669= NM_172198.3:c.1106+72668_1106+72669del NM_172198.3:c.1106+72669del NM_172198.3:c.1106+72669dup NM_172198.3:c.1106+72668_1106+72669dup NM_172198.3:c.1106+72667_1106+72669dup NM_172198.3:c.1106+72666_1106+72669dup
KCND3 transcript variant X1 XM_005270851.1:c.1106+72669= XM_005270851.1:c.1106+72668_1106+72669del XM_005270851.1:c.1106+72669del XM_005270851.1:c.1106+72669dup XM_005270851.1:c.1106+72668_1106+72669dup XM_005270851.1:c.1106+72667_1106+72669dup XM_005270851.1:c.1106+72666_1106+72669dup
KCND3 transcript variant X2 XM_005270852.1:c.1106+72669= XM_005270852.1:c.1106+72668_1106+72669del XM_005270852.1:c.1106+72669del XM_005270852.1:c.1106+72669dup XM_005270852.1:c.1106+72668_1106+72669dup XM_005270852.1:c.1106+72667_1106+72669dup XM_005270852.1:c.1106+72666_1106+72669dup
KCND3 transcript variant X3 XM_005270853.1:c.1106+72669= XM_005270853.1:c.1106+72668_1106+72669del XM_005270853.1:c.1106+72669del XM_005270853.1:c.1106+72669dup XM_005270853.1:c.1106+72668_1106+72669dup XM_005270853.1:c.1106+72667_1106+72669dup XM_005270853.1:c.1106+72666_1106+72669dup
KCND3 transcript variant X4 XM_005270854.1:c.1106+72669= XM_005270854.1:c.1106+72668_1106+72669del XM_005270854.1:c.1106+72669del XM_005270854.1:c.1106+72669dup XM_005270854.1:c.1106+72668_1106+72669dup XM_005270854.1:c.1106+72667_1106+72669dup XM_005270854.1:c.1106+72666_1106+72669dup
KCND3 transcript variant X5 XM_005270855.1:c.1106+72669= XM_005270855.1:c.1106+72668_1106+72669del XM_005270855.1:c.1106+72669del XM_005270855.1:c.1106+72669dup XM_005270855.1:c.1106+72668_1106+72669dup XM_005270855.1:c.1106+72667_1106+72669dup XM_005270855.1:c.1106+72666_1106+72669dup
KCND3 transcript variant X1 XM_006710629.5:c.1106+72669= XM_006710629.5:c.1106+72668_1106+72669del XM_006710629.5:c.1106+72669del XM_006710629.5:c.1106+72669dup XM_006710629.5:c.1106+72668_1106+72669dup XM_006710629.5:c.1106+72667_1106+72669dup XM_006710629.5:c.1106+72666_1106+72669dup
KCND3 transcript variant X6 XM_006710632.4:c.1107-12961= XM_006710632.4:c.1107-12962_1107-12961del XM_006710632.4:c.1107-12961del XM_006710632.4:c.1107-12961dup XM_006710632.4:c.1107-12962_1107-12961dup XM_006710632.4:c.1107-12963_1107-12961dup XM_006710632.4:c.1107-12964_1107-12961dup
KCND3 transcript variant X7 XM_011541427.4:c.1106+72669= XM_011541427.4:c.1106+72668_1106+72669del XM_011541427.4:c.1106+72669del XM_011541427.4:c.1106+72669dup XM_011541427.4:c.1106+72668_1106+72669dup XM_011541427.4:c.1106+72667_1106+72669dup XM_011541427.4:c.1106+72666_1106+72669dup
KCND3 transcript variant X2 XM_017001244.3:c.1106+72669= XM_017001244.3:c.1106+72668_1106+72669del XM_017001244.3:c.1106+72669del XM_017001244.3:c.1106+72669dup XM_017001244.3:c.1106+72668_1106+72669dup XM_017001244.3:c.1106+72667_1106+72669dup XM_017001244.3:c.1106+72666_1106+72669dup
Help

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#.

56 SubSNP, 24 Frequency submissions
No Submitter Submission ID Date (Build)
1 TSC-CSHL ss4290157 Mar 15, 2016 (147)
2 ABI ss41120975 Mar 13, 2006 (126)
3 ABI ss41135850 Mar 15, 2006 (126)
4 HGSV ss83858451 Dec 14, 2007 (137)
5 HUMANGENOME_JCVI ss95240508 Feb 06, 2009 (137)
6 HUMANGENOME_JCVI ss98575208 Feb 06, 2009 (130)
7 GMI ss288027486 May 04, 2012 (137)
8 PJP ss294598646 May 09, 2011 (137)
9 SSMP ss663110331 Apr 01, 2015 (144)
10 BILGI_BIOE ss666106406 Apr 25, 2013 (138)
11 1000GENOMES ss1367817592 Aug 21, 2014 (142)
12 EVA_UK10K_TWINSUK ss1701111852 Apr 01, 2015 (144)
13 EVA_UK10K_TWINSUK ss1701111856 Apr 01, 2015 (144)
14 EVA_UK10K_ALSPAC ss1701111956 Apr 01, 2015 (144)
15 EVA_UK10K_ALSPAC ss1701111959 Apr 01, 2015 (144)
16 SWEGEN ss2987445895 Nov 08, 2017 (151)
17 EVA_DECODE ss3687539631 Jul 12, 2019 (153)
18 EVA_DECODE ss3687539632 Jul 12, 2019 (153)
19 EVA_DECODE ss3687539633 Jul 12, 2019 (153)
20 EVA_DECODE ss3687539634 Jul 12, 2019 (153)
21 PACBIO ss3783520841 Jul 12, 2019 (153)
22 PACBIO ss3789162468 Jul 12, 2019 (153)
23 PACBIO ss3794035393 Jul 12, 2019 (153)
24 KHV_HUMAN_GENOMES ss3799681347 Jul 12, 2019 (153)
25 EVA ss3826372250 Apr 25, 2020 (154)
26 EVA ss3836577784 Apr 25, 2020 (154)
27 EVA ss3841986169 Apr 25, 2020 (154)
28 KOGIC ss3945256039 Apr 25, 2020 (154)
29 KOGIC ss3945256040 Apr 25, 2020 (154)
30 KOGIC ss3945256041 Apr 25, 2020 (154)
31 KOGIC ss3945256042 Apr 25, 2020 (154)
32 GNOMAD ss4000516102 Apr 25, 2021 (155)
33 GNOMAD ss4000516103 Apr 25, 2021 (155)
34 GNOMAD ss4000516104 Apr 25, 2021 (155)
35 GNOMAD ss4000516105 Apr 25, 2021 (155)
36 GNOMAD ss4000516107 Apr 25, 2021 (155)
37 GNOMAD ss4000516108 Apr 25, 2021 (155)
38 TOMMO_GENOMICS ss5145699842 Apr 25, 2021 (155)
39 TOMMO_GENOMICS ss5145699843 Apr 25, 2021 (155)
40 TOMMO_GENOMICS ss5145699844 Apr 25, 2021 (155)
41 TOMMO_GENOMICS ss5145699845 Apr 25, 2021 (155)
42 1000G_HIGH_COVERAGE ss5243624456 Oct 12, 2022 (156)
43 1000G_HIGH_COVERAGE ss5243624457 Oct 12, 2022 (156)
44 1000G_HIGH_COVERAGE ss5243624458 Oct 12, 2022 (156)
45 1000G_HIGH_COVERAGE ss5243624459 Oct 12, 2022 (156)
46 1000G_HIGH_COVERAGE ss5243624460 Oct 12, 2022 (156)
47 HUGCELL_USP ss5444547112 Oct 12, 2022 (156)
48 HUGCELL_USP ss5444547113 Oct 12, 2022 (156)
49 HUGCELL_USP ss5444547114 Oct 12, 2022 (156)
50 HUGCELL_USP ss5444547115 Oct 12, 2022 (156)
51 TOMMO_GENOMICS ss5670973053 Oct 12, 2022 (156)
52 TOMMO_GENOMICS ss5670973054 Oct 12, 2022 (156)
53 TOMMO_GENOMICS ss5670973055 Oct 12, 2022 (156)
54 TOMMO_GENOMICS ss5670973056 Oct 12, 2022 (156)
55 EVA ss5832490431 Oct 12, 2022 (156)
56 EVA ss5832490432 Oct 12, 2022 (156)
57 1000Genomes NC_000001.10 - 112451574 Oct 11, 2018 (152)
58 The Avon Longitudinal Study of Parents and Children

Submission ignored due to conflicting rows:
Row 1785790 (NC_000001.10:112451573::T 1774/3854)
Row 1785791 (NC_000001.10:112451573::TT 306/3854)

- Oct 11, 2018 (152)
59 The Avon Longitudinal Study of Parents and Children

Submission ignored due to conflicting rows:
Row 1785790 (NC_000001.10:112451573::T 1774/3854)
Row 1785791 (NC_000001.10:112451573::TT 306/3854)

- Oct 11, 2018 (152)
60 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 22819705 (NC_000001.11:111908951::T 56810/120542)
Row 22819706 (NC_000001.11:111908951::TT 9497/120562)
Row 22819707 (NC_000001.11:111908951::TTT 1274/120596)...

- Apr 25, 2021 (155)
61 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 22819705 (NC_000001.11:111908951::T 56810/120542)
Row 22819706 (NC_000001.11:111908951::TT 9497/120562)
Row 22819707 (NC_000001.11:111908951::TTT 1274/120596)...

- Apr 25, 2021 (155)
62 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 22819705 (NC_000001.11:111908951::T 56810/120542)
Row 22819706 (NC_000001.11:111908951::TT 9497/120562)
Row 22819707 (NC_000001.11:111908951::TTT 1274/120596)...

- Apr 25, 2021 (155)
63 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 22819705 (NC_000001.11:111908951::T 56810/120542)
Row 22819706 (NC_000001.11:111908951::TT 9497/120562)
Row 22819707 (NC_000001.11:111908951::TTT 1274/120596)...

- Apr 25, 2021 (155)
64 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 22819705 (NC_000001.11:111908951::T 56810/120542)
Row 22819706 (NC_000001.11:111908951::TT 9497/120562)
Row 22819707 (NC_000001.11:111908951::TTT 1274/120596)...

- Apr 25, 2021 (155)
65 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 22819705 (NC_000001.11:111908951::T 56810/120542)
Row 22819706 (NC_000001.11:111908951::TT 9497/120562)
Row 22819707 (NC_000001.11:111908951::TTT 1274/120596)...

- Apr 25, 2021 (155)
66 Korean Genome Project

Submission ignored due to conflicting rows:
Row 1634040 (NC_000001.11:111908952::T 453/1828)
Row 1634041 (NC_000001.11:111908952::TT 519/1828)
Row 1634042 (NC_000001.11:111908951:T: 44/1828)...

- Apr 25, 2020 (154)
67 Korean Genome Project

Submission ignored due to conflicting rows:
Row 1634040 (NC_000001.11:111908952::T 453/1828)
Row 1634041 (NC_000001.11:111908952::TT 519/1828)
Row 1634042 (NC_000001.11:111908951:T: 44/1828)...

- Apr 25, 2020 (154)
68 Korean Genome Project

Submission ignored due to conflicting rows:
Row 1634040 (NC_000001.11:111908952::T 453/1828)
Row 1634041 (NC_000001.11:111908952::TT 519/1828)
Row 1634042 (NC_000001.11:111908951:T: 44/1828)...

- Apr 25, 2020 (154)
69 Korean Genome Project

Submission ignored due to conflicting rows:
Row 1634040 (NC_000001.11:111908952::T 453/1828)
Row 1634041 (NC_000001.11:111908952::TT 519/1828)
Row 1634042 (NC_000001.11:111908951:T: 44/1828)...

- Apr 25, 2020 (154)
70 8.3KJPN

Submission ignored due to conflicting rows:
Row 3669149 (NC_000001.10:112451573::TT 4096/16684)
Row 3669150 (NC_000001.10:112451573::T 4034/16684)
Row 3669151 (NC_000001.10:112451573::TTT 11/16684)...

- Apr 25, 2021 (155)
71 8.3KJPN

Submission ignored due to conflicting rows:
Row 3669149 (NC_000001.10:112451573::TT 4096/16684)
Row 3669150 (NC_000001.10:112451573::T 4034/16684)
Row 3669151 (NC_000001.10:112451573::TTT 11/16684)...

- Apr 25, 2021 (155)
72 8.3KJPN

Submission ignored due to conflicting rows:
Row 3669149 (NC_000001.10:112451573::TT 4096/16684)
Row 3669150 (NC_000001.10:112451573::T 4034/16684)
Row 3669151 (NC_000001.10:112451573::TTT 11/16684)...

- Apr 25, 2021 (155)
73 8.3KJPN

Submission ignored due to conflicting rows:
Row 3669149 (NC_000001.10:112451573::TT 4096/16684)
Row 3669150 (NC_000001.10:112451573::T 4034/16684)
Row 3669151 (NC_000001.10:112451573::TTT 11/16684)...

- Apr 25, 2021 (155)
74 14KJPN

Submission ignored due to conflicting rows:
Row 4810157 (NC_000001.11:111908951::TT 7158/28252)
Row 4810158 (NC_000001.11:111908951::T 6911/28252)
Row 4810159 (NC_000001.11:111908951:T: 23/28252)...

- Oct 12, 2022 (156)
75 14KJPN

Submission ignored due to conflicting rows:
Row 4810157 (NC_000001.11:111908951::TT 7158/28252)
Row 4810158 (NC_000001.11:111908951::T 6911/28252)
Row 4810159 (NC_000001.11:111908951:T: 23/28252)...

- Oct 12, 2022 (156)
76 14KJPN

Submission ignored due to conflicting rows:
Row 4810157 (NC_000001.11:111908951::TT 7158/28252)
Row 4810158 (NC_000001.11:111908951::T 6911/28252)
Row 4810159 (NC_000001.11:111908951:T: 23/28252)...

- Oct 12, 2022 (156)
77 14KJPN

Submission ignored due to conflicting rows:
Row 4810157 (NC_000001.11:111908951::TT 7158/28252)
Row 4810158 (NC_000001.11:111908951::T 6911/28252)
Row 4810159 (NC_000001.11:111908951:T: 23/28252)...

- Oct 12, 2022 (156)
78 UK 10K study - Twins

Submission ignored due to conflicting rows:
Row 1785790 (NC_000001.10:112451573::T 1753/3708)
Row 1785791 (NC_000001.10:112451573::TT 300/3708)

- Oct 11, 2018 (152)
79 UK 10K study - Twins

Submission ignored due to conflicting rows:
Row 1785790 (NC_000001.10:112451573::T 1753/3708)
Row 1785791 (NC_000001.10:112451573::TT 300/3708)

- Oct 11, 2018 (152)
80 ALFA NC_000001.11 - 111908952 Apr 25, 2021 (155)
Help

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)
rs57602351 May 11, 2012 (137)
rs149090534 Sep 17, 2011 (135)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss4000516108 NC_000001.11:111908951:TT: NC_000001.11:111908951:TTTTTTTTTTT…

NC_000001.11:111908951:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT

(self)
4042317700 NC_000001.11:111908951:TTTTTTTTTTT…

NC_000001.11:111908951:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT

NC_000001.11:111908951:TTTTTTTTTTT…

NC_000001.11:111908951:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT

(self)
ss2987445895, ss5145699845 NC_000001.10:112451573:T: NC_000001.11:111908951:TTTTTTTTTTT…

NC_000001.11:111908951:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT

(self)
ss3687539631, ss3945256041, ss4000516107, ss5243624458, ss5444547112, ss5670973055 NC_000001.11:111908951:T: NC_000001.11:111908951:TTTTTTTTTTT…

NC_000001.11:111908951:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT

(self)
4042317700 NC_000001.11:111908951:TTTTTTTTTTT…

NC_000001.11:111908951:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT

NC_000001.11:111908951:TTTTTTTTTTT…

NC_000001.11:111908951:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT

(self)
ss4290157 NT_032977.9:82423506:T: NC_000001.11:111908951:TTTTTTTTTTT…

NC_000001.11:111908951:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT

(self)
ss288027486, ss294598646 NC_000001.9:112253112::T NC_000001.11:111908951:TTTTTTTTTTT…

NC_000001.11:111908951:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT

(self)
3227718, ss666106406, ss1367817592, ss1701111852, ss1701111956, ss3783520841, ss3789162468, ss3794035393, ss3826372250, ss3836577784, ss5145699843, ss5832490431 NC_000001.10:112451573::T NC_000001.11:111908951:TTTTTTTTTTT…

NC_000001.11:111908951:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT

(self)
ss3799681347, ss3841986169, ss4000516102, ss5243624456, ss5444547113, ss5670973054 NC_000001.11:111908951::T NC_000001.11:111908951:TTTTTTTTTTT…

NC_000001.11:111908951:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT

(self)
4042317700 NC_000001.11:111908951:TTTTTTTTTTT…

NC_000001.11:111908951:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT

NC_000001.11:111908951:TTTTTTTTTTT…

NC_000001.11:111908951:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT

(self)
ss3687539632, ss3945256039 NC_000001.11:111908952::T NC_000001.11:111908951:TTTTTTTTTTT…

NC_000001.11:111908951:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT

(self)
ss41135850, ss98575208 NT_032977.9:82423491::T NC_000001.11:111908951:TTTTTTTTTTT…

NC_000001.11:111908951:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT

(self)
ss41120975 NT_032977.9:82423492::T NC_000001.11:111908951:TTTTTTTTTTT…

NC_000001.11:111908951:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT

(self)
ss4290157 NT_032977.9:82423506:T:TT NC_000001.11:111908951:TTTTTTTTTTT…

NC_000001.11:111908951:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT

(self)
ss83858451, ss95240508 NT_032977.9:82423507::T NC_000001.11:111908951:TTTTTTTTTTT…

NC_000001.11:111908951:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT

(self)
ss663110331, ss1701111856, ss1701111959, ss5145699842, ss5832490432 NC_000001.10:112451573::TT NC_000001.11:111908951:TTTTTTTTTTT…

NC_000001.11:111908951:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT

(self)
ss4000516103, ss5243624457, ss5444547114, ss5670973053 NC_000001.11:111908951::TT NC_000001.11:111908951:TTTTTTTTTTT…

NC_000001.11:111908951:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT

(self)
4042317700 NC_000001.11:111908951:TTTTTTTTTTT…

NC_000001.11:111908951:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT

NC_000001.11:111908951:TTTTTTTTTTT…

NC_000001.11:111908951:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT

(self)
ss3687539633, ss3945256040 NC_000001.11:111908952::TT NC_000001.11:111908951:TTTTTTTTTTT…

NC_000001.11:111908951:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT

(self)
ss5145699844 NC_000001.10:112451573::TTT NC_000001.11:111908951:TTTTTTTTTTT…

NC_000001.11:111908951:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT

(self)
ss4000516104, ss5243624459, ss5444547115, ss5670973056 NC_000001.11:111908951::TTT NC_000001.11:111908951:TTTTTTTTTTT…

NC_000001.11:111908951:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT

(self)
4042317700 NC_000001.11:111908951:TTTTTTTTTTT…

NC_000001.11:111908951:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT

NC_000001.11:111908951:TTTTTTTTTTT…

NC_000001.11:111908951:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT

(self)
ss3687539634, ss3945256042 NC_000001.11:111908952::TTT NC_000001.11:111908951:TTTTTTTTTTT…

NC_000001.11:111908951:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT

(self)
ss4000516105, ss5243624460 NC_000001.11:111908951::TTTT NC_000001.11:111908951:TTTTTTTTTTT…

NC_000001.11:111908951:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT

(self)
4042317700 NC_000001.11:111908951:TTTTTTTTTTT…

NC_000001.11:111908951:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT

NC_000001.11:111908951:TTTTTTTTTTT…

NC_000001.11:111908951:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT

(self)
Help

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

No publications for rs34151345

Help

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.

Software version is: 2.0.1.post820+afb47a3d