Name: rs34372202
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.

rs34372202

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr7:154535387-154535398 (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)₄ / delTTT / delTT / delT / …
del(T)₄ / delTTT / delTT / delT / dupT / dupTT
Variation Type: Indel Insertion and Deletion
Frequency: delT=0.2713 (1375/5069, ALFA)
dupT=0.4163 (2085/5008, 1000G)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: DPP6 : 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	5069	TTTTTTTTTTTT=0.2602	TTTTTTTT=0.0000, TTTTTTTTT=0.0000, TTTTTTTTTT=0.0582, TTTTTTTTTTT=0.2713, TTTTTTTTTTTTT=0.4103, TTTTTTTTTTTTTT=0.0000	0.168648	0.384844	0.446508	3
European	Sub	4667	TTTTTTTTTTTT=0.1976	TTTTTTTT=0.0000, TTTTTTTTT=0.0000, TTTTTTTTTT=0.0632, TTTTTTTTTTT=0.2938, TTTTTTTTTTTTT=0.4455, TTTTTTTTTTTTTT=0.0000	0.168155	0.385417	0.446429	3
African	Sub	288	TTTTTTTTTTTT=1.000	TTTTTTTT=0.000, TTTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000	0	0	0	N/A
African Others	Sub	14	TTTTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00	0	0	0	N/A
African American	Sub	274	TTTTTTTTTTTT=1.000	TTTTTTTT=0.000, TTTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000	0	0	0	N/A
Asian	Sub	30	TTTTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00	0	0	0	N/A
East Asian	Sub	28	TTTTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00	0	0	0	N/A
Other Asian	Sub	2	TTTTTTTTTTTT=1.0	TTTTTTTT=0.0, TTTTTTTTT=0.0, TTTTTTTTTT=0.0, TTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0	0	0	0	N/A
Latin American 1	Sub	4	TTTTTTTTTTTT=1.0	TTTTTTTT=0.0, TTTTTTTTT=0.0, TTTTTTTTTT=0.0, TTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0	0	0	0	N/A
Latin American 2	Sub	34	TTTTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00	0	0	0	N/A
South Asian	Sub	8	TTTTTTTTTTTT=1.0	TTTTTTTT=0.0, TTTTTTTTT=0.0, TTTTTTTTTT=0.0, TTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0	0	0	0	N/A
Other	Sub	38	TTTTTTTTTTTT=0.87	TTTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.11, TTTTTTTTTTTTT=0.03, TTTTTTTTTTTTTT=0.00	0.5	0.0	0.5	0

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	5069	(T)₁₂=0.2602	del(T)₄=0.0000, delTTT=0.0000, delTT=0.0582, delT=0.2713, dupT=0.4103, dupTT=0.0000
Allele Frequency Aggregator	European	Sub	4667	(T)₁₂=0.1976	del(T)₄=0.0000, delTTT=0.0000, delTT=0.0632, delT=0.2938, dupT=0.4455, dupTT=0.0000
Allele Frequency Aggregator	African	Sub	288	(T)₁₂=1.000	del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000
Allele Frequency Aggregator	Other	Sub	38	(T)₁₂=0.87	del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.11, dupT=0.03, dupTT=0.00
Allele Frequency Aggregator	Latin American 2	Sub	34	(T)₁₂=1.00	del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00
Allele Frequency Aggregator	Asian	Sub	30	(T)₁₂=1.00	del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00
Allele Frequency Aggregator	South Asian	Sub	8	(T)₁₂=1.0	del(T)₄=0.0, delTTT=0.0, delTT=0.0, delT=0.0, dupT=0.0, dupTT=0.0
Allele Frequency Aggregator	Latin American 1	Sub	4	(T)₁₂=1.0	del(T)₄=0.0, delTTT=0.0, delTT=0.0, delT=0.0, dupT=0.0, dupTT=0.0
1000Genomes	Global	Study-wide	5008	- No frequency provided	dupT=0.4163
1000Genomes	African	Sub	1322	- No frequency provided	dupT=0.1770
1000Genomes	East Asian	Sub	1008	- No frequency provided	dupT=0.4048
1000Genomes	Europe	Sub	1006	- No frequency provided	dupT=0.5755
1000Genomes	South Asian	Sub	978	- No frequency provided	dupT=0.462
1000Genomes	American	Sub	694	- No frequency provided	dupT=0.594

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 7	NC_000007.14:g.154535395_154535398del
GRCh38.p14 chr 7	NC_000007.14:g.154535396_154535398del
GRCh38.p14 chr 7	NC_000007.14:g.154535397_154535398del
GRCh38.p14 chr 7	NC_000007.14:g.154535398del
GRCh38.p14 chr 7	NC_000007.14:g.154535398dup
GRCh38.p14 chr 7	NC_000007.14:g.154535397_154535398dup
GRCh37.p13 chr 7	NC_000007.13:g.154232480_154232483del
GRCh37.p13 chr 7	NC_000007.13:g.154232481_154232483del
GRCh37.p13 chr 7	NC_000007.13:g.154232482_154232483del
GRCh37.p13 chr 7	NC_000007.13:g.154232483del
GRCh37.p13 chr 7	NC_000007.13:g.154232483dup
GRCh37.p13 chr 7	NC_000007.13:g.154232482_154232483dup
DPP6 RefSeqGene	NG_033878.2:g.792410_792413del
DPP6 RefSeqGene	NG_033878.2:g.792411_792413del
DPP6 RefSeqGene	NG_033878.2:g.792412_792413del
DPP6 RefSeqGene	NG_033878.2:g.792413del
DPP6 RefSeqGene	NG_033878.2:g.792413dup
DPP6 RefSeqGene	NG_033878.2:g.792412_792413dup
GRCh38.p14 chr 7 fix patch HG2239_PATCH	NW_012132919.1:g.113044_113047del
GRCh38.p14 chr 7 fix patch HG2239_PATCH	NW_012132919.1:g.113045_113047del
GRCh38.p14 chr 7 fix patch HG2239_PATCH	NW_012132919.1:g.113046_113047del
GRCh38.p14 chr 7 fix patch HG2239_PATCH	NW_012132919.1:g.113047del
GRCh38.p14 chr 7 fix patch HG2239_PATCH	NW_012132919.1:g.113047dup
GRCh38.p14 chr 7 fix patch HG2239_PATCH	NW_012132919.1:g.113046_113047dup

Gene: DPP6, dipeptidyl peptidase like 6 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
DPP6 transcript variant 3	NM_001039350.3:c.266-5137… NM_001039350.3:c.266-5137_266-5134del	N/A	Intron Variant
DPP6 transcript variant 4	NM_001290252.2:c.272-5137… NM_001290252.2:c.272-5137_272-5134del	N/A	Intron Variant
DPP6 transcript variant 5	NM_001290253.2:c.458-5137… NM_001290253.2:c.458-5137_458-5134del	N/A	Intron Variant
DPP6 transcript variant 6	NM_001364497.2:c.275-5137… NM_001364497.2:c.275-5137_275-5134del	N/A	Intron Variant
DPP6 transcript variant 7	NM_001364498.2:c.275-5137… NM_001364498.2:c.275-5137_275-5134del	N/A	Intron Variant
DPP6 transcript variant 8	NM_001364499.2:c.275-5137… NM_001364499.2:c.275-5137_275-5134del	N/A	Intron Variant
DPP6 transcript variant 9	NM_001364500.2:c.275-5137… NM_001364500.2:c.275-5137_275-5134del	N/A	Intron Variant
DPP6 transcript variant 10	NM_001364501.2:c.266-5137… NM_001364501.2:c.266-5137_266-5134del	N/A	Intron Variant
DPP6 transcript variant 11	NM_001364502.2:c.272-5137… NM_001364502.2:c.272-5137_272-5134del	N/A	Intron Variant
DPP6 transcript variant 2	NM_001936.5:c.272-5137_27… NM_001936.5:c.272-5137_272-5134del	N/A	Intron Variant
DPP6 transcript variant 1	NM_130797.4:c.458-5137_45… NM_130797.4:c.458-5137_458-5134del	N/A	Intron Variant
DPP6 transcript variant 12	NR_157195.2:n.	N/A	Intron Variant
DPP6 transcript variant 13	NR_157196.2:n.	N/A	Intron Variant
DPP6 transcript variant X2	XM_047419951.1:c.275-5137… XM_047419951.1:c.275-5137_275-5134del	N/A	Intron Variant
DPP6 transcript variant X1	XM_017011812.3:c.	N/A	Genic 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)₁₂=	del(T)₄	delTTT	delTT	delT	dupT	dupTT
GRCh38.p14 chr 7	NC_000007.14:g.154535387_154535398=	NC_000007.14:g.154535395_154535398del	NC_000007.14:g.154535396_154535398del	NC_000007.14:g.154535397_154535398del	NC_000007.14:g.154535398del	NC_000007.14:g.154535398dup	NC_000007.14:g.154535397_154535398dup
GRCh37.p13 chr 7	NC_000007.13:g.154232472_154232483=	NC_000007.13:g.154232480_154232483del	NC_000007.13:g.154232481_154232483del	NC_000007.13:g.154232482_154232483del	NC_000007.13:g.154232483del	NC_000007.13:g.154232483dup	NC_000007.13:g.154232482_154232483dup
DPP6 RefSeqGene	NG_033878.2:g.792402_792413=	NG_033878.2:g.792410_792413del	NG_033878.2:g.792411_792413del	NG_033878.2:g.792412_792413del	NG_033878.2:g.792413del	NG_033878.2:g.792413dup	NG_033878.2:g.792412_792413dup
GRCh38.p14 chr 7 fix patch HG2239_PATCH	NW_012132919.1:g.113036_113047=	NW_012132919.1:g.113044_113047del	NW_012132919.1:g.113045_113047del	NW_012132919.1:g.113046_113047del	NW_012132919.1:g.113047del	NW_012132919.1:g.113047dup	NW_012132919.1:g.113046_113047dup
DPP6 transcript variant 3	NM_001039350.1:c.266-5145=	NM_001039350.1:c.266-5137_266-5134del	NM_001039350.1:c.266-5136_266-5134del	NM_001039350.1:c.266-5135_266-5134del	NM_001039350.1:c.266-5134del	NM_001039350.1:c.266-5134dup	NM_001039350.1:c.266-5135_266-5134dup
DPP6 transcript variant 3	NM_001039350.3:c.266-5145=	NM_001039350.3:c.266-5137_266-5134del	NM_001039350.3:c.266-5136_266-5134del	NM_001039350.3:c.266-5135_266-5134del	NM_001039350.3:c.266-5134del	NM_001039350.3:c.266-5134dup	NM_001039350.3:c.266-5135_266-5134dup
DPP6 transcript variant 4	NM_001290252.2:c.272-5145=	NM_001290252.2:c.272-5137_272-5134del	NM_001290252.2:c.272-5136_272-5134del	NM_001290252.2:c.272-5135_272-5134del	NM_001290252.2:c.272-5134del	NM_001290252.2:c.272-5134dup	NM_001290252.2:c.272-5135_272-5134dup
DPP6 transcript variant 5	NM_001290253.2:c.458-5145=	NM_001290253.2:c.458-5137_458-5134del	NM_001290253.2:c.458-5136_458-5134del	NM_001290253.2:c.458-5135_458-5134del	NM_001290253.2:c.458-5134del	NM_001290253.2:c.458-5134dup	NM_001290253.2:c.458-5135_458-5134dup
DPP6 transcript variant 6	NM_001364497.2:c.275-5145=	NM_001364497.2:c.275-5137_275-5134del	NM_001364497.2:c.275-5136_275-5134del	NM_001364497.2:c.275-5135_275-5134del	NM_001364497.2:c.275-5134del	NM_001364497.2:c.275-5134dup	NM_001364497.2:c.275-5135_275-5134dup
DPP6 transcript variant 7	NM_001364498.2:c.275-5145=	NM_001364498.2:c.275-5137_275-5134del	NM_001364498.2:c.275-5136_275-5134del	NM_001364498.2:c.275-5135_275-5134del	NM_001364498.2:c.275-5134del	NM_001364498.2:c.275-5134dup	NM_001364498.2:c.275-5135_275-5134dup
DPP6 transcript variant 8	NM_001364499.2:c.275-5145=	NM_001364499.2:c.275-5137_275-5134del	NM_001364499.2:c.275-5136_275-5134del	NM_001364499.2:c.275-5135_275-5134del	NM_001364499.2:c.275-5134del	NM_001364499.2:c.275-5134dup	NM_001364499.2:c.275-5135_275-5134dup
DPP6 transcript variant 9	NM_001364500.2:c.275-5145=	NM_001364500.2:c.275-5137_275-5134del	NM_001364500.2:c.275-5136_275-5134del	NM_001364500.2:c.275-5135_275-5134del	NM_001364500.2:c.275-5134del	NM_001364500.2:c.275-5134dup	NM_001364500.2:c.275-5135_275-5134dup
DPP6 transcript variant 10	NM_001364501.2:c.266-5145=	NM_001364501.2:c.266-5137_266-5134del	NM_001364501.2:c.266-5136_266-5134del	NM_001364501.2:c.266-5135_266-5134del	NM_001364501.2:c.266-5134del	NM_001364501.2:c.266-5134dup	NM_001364501.2:c.266-5135_266-5134dup
DPP6 transcript variant 11	NM_001364502.2:c.272-5145=	NM_001364502.2:c.272-5137_272-5134del	NM_001364502.2:c.272-5136_272-5134del	NM_001364502.2:c.272-5135_272-5134del	NM_001364502.2:c.272-5134del	NM_001364502.2:c.272-5134dup	NM_001364502.2:c.272-5135_272-5134dup
DPP6 transcript variant 2	NM_001936.3:c.272-5145=	NM_001936.3:c.272-5137_272-5134del	NM_001936.3:c.272-5136_272-5134del	NM_001936.3:c.272-5135_272-5134del	NM_001936.3:c.272-5134del	NM_001936.3:c.272-5134dup	NM_001936.3:c.272-5135_272-5134dup
DPP6 transcript variant 2	NM_001936.5:c.272-5145=	NM_001936.5:c.272-5137_272-5134del	NM_001936.5:c.272-5136_272-5134del	NM_001936.5:c.272-5135_272-5134del	NM_001936.5:c.272-5134del	NM_001936.5:c.272-5134dup	NM_001936.5:c.272-5135_272-5134dup
DPP6 transcript variant 1	NM_130797.2:c.458-5145=	NM_130797.2:c.458-5137_458-5134del	NM_130797.2:c.458-5136_458-5134del	NM_130797.2:c.458-5135_458-5134del	NM_130797.2:c.458-5134del	NM_130797.2:c.458-5134dup	NM_130797.2:c.458-5135_458-5134dup
DPP6 transcript variant 1	NM_130797.4:c.458-5145=	NM_130797.4:c.458-5137_458-5134del	NM_130797.4:c.458-5136_458-5134del	NM_130797.4:c.458-5135_458-5134del	NM_130797.4:c.458-5134del	NM_130797.4:c.458-5134dup	NM_130797.4:c.458-5135_458-5134dup
DPP6 transcript variant X2	XM_047419951.1:c.275-5145=	XM_047419951.1:c.275-5137_275-5134del	XM_047419951.1:c.275-5136_275-5134del	XM_047419951.1:c.275-5135_275-5134del	XM_047419951.1:c.275-5134del	XM_047419951.1:c.275-5134dup	XM_047419951.1:c.275-5135_275-5134dup

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#.

65 SubSNP, 19 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss42927005	Mar 13, 2006 (126)
2	ABI	ss42931638	Dec 03, 2013 (138)
3	ABI	ss42979961	Dec 03, 2013 (138)
4	HGSV	ss79812677	Sep 08, 2015 (146)
5	HUMANGENOME_JCVI	ss95480412	Feb 03, 2009 (130)
6	HUMANGENOME_JCVI	ss98216373	Mar 15, 2016 (147)
7	BGI	ss104781544	Mar 15, 2016 (151)
8	BGI	ss105539452	Mar 15, 2016 (151)
9	BUSHMAN	ss193955671	Jul 04, 2010 (132)
10	GMI	ss287823895	May 09, 2011 (134)
11	GMI	ss288882844	May 04, 2012 (137)
12	GMI	ss288882845	May 04, 2012 (138)
13	PJP	ss295363852	Jan 10, 2018 (151)
14	PJP	ss295363853	May 09, 2011 (137)
15	PJP	ss295363854	May 09, 2011 (138)
16	SSMP	ss663759858	Apr 01, 2015 (144)
17	BILGI_BIOE	ss666423281	Apr 25, 2013 (138)
18	1000GENOMES	ss1367796575	Aug 21, 2014 (142)
19	SWEGEN	ss3002346432	Jan 10, 2018 (151)
20	MCHAISSO	ss3066180097	Jan 10, 2018 (151)
21	BEROUKHIMLAB	ss3644252481	Oct 12, 2018 (152)
22	BIOINF_KMB_FNS_UNIBA	ss3646068709	Oct 12, 2018 (152)
23	BIOINF_KMB_FNS_UNIBA	ss3646068710	Oct 12, 2018 (152)
24	EVA_DECODE	ss3721049271	Jul 13, 2019 (153)
25	EVA_DECODE	ss3721049272	Jul 13, 2019 (153)
26	EVA_DECODE	ss3721049273	Jul 13, 2019 (153)
27	EVA_DECODE	ss3721049274	Jul 13, 2019 (153)
28	PACBIO	ss3786010107	Jul 13, 2019 (153)
29	PACBIO	ss3791281028	Jul 13, 2019 (153)
30	PACBIO	ss3796161369	Jul 13, 2019 (153)
31	KHV_HUMAN_GENOMES	ss3810548900	Jul 13, 2019 (153)
32	EVA	ss3830911600	Apr 26, 2020 (154)
33	EVA	ss3838957093	Apr 26, 2020 (154)
34	EVA	ss3844414851	Apr 26, 2020 (154)
35	KOGIC	ss3962934582	Apr 26, 2020 (154)
36	KOGIC	ss3962934583	Apr 26, 2020 (154)
37	KOGIC	ss3962934584	Apr 26, 2020 (154)
38	GNOMAD	ss4176235711	Apr 26, 2021 (155)
39	GNOMAD	ss4176235712	Apr 26, 2021 (155)
40	GNOMAD	ss4176235714	Apr 26, 2021 (155)
41	GNOMAD	ss4176235715	Apr 26, 2021 (155)
42	GNOMAD	ss4176235716	Apr 26, 2021 (155)
43	GNOMAD	ss4176235717	Apr 26, 2021 (155)
44	TOMMO_GENOMICS	ss5186417432	Apr 26, 2021 (155)
45	TOMMO_GENOMICS	ss5186417433	Apr 26, 2021 (155)
46	TOMMO_GENOMICS	ss5186417434	Apr 26, 2021 (155)
47	TOMMO_GENOMICS	ss5186417435	Apr 26, 2021 (155)
48	1000G_HIGH_COVERAGE	ss5275390731	Oct 16, 2022 (156)
49	1000G_HIGH_COVERAGE	ss5275390732	Oct 16, 2022 (156)
50	1000G_HIGH_COVERAGE	ss5275390733	Oct 16, 2022 (156)
51	1000G_HIGH_COVERAGE	ss5275390734	Oct 16, 2022 (156)
52	1000G_HIGH_COVERAGE	ss5275390735	Oct 16, 2022 (156)
53	1000G_HIGH_COVERAGE	ss5275390736	Oct 16, 2022 (156)
54	HUGCELL_USP	ss5472183454	Oct 16, 2022 (156)
55	HUGCELL_USP	ss5472183455	Oct 16, 2022 (156)
56	HUGCELL_USP	ss5472183456	Oct 16, 2022 (156)
57	HUGCELL_USP	ss5472183457	Oct 16, 2022 (156)
58	HUGCELL_USP	ss5472183458	Oct 16, 2022 (156)
59	TOMMO_GENOMICS	ss5727675012	Oct 16, 2022 (156)
60	TOMMO_GENOMICS	ss5727675013	Oct 16, 2022 (156)
61	TOMMO_GENOMICS	ss5727675014	Oct 16, 2022 (156)
62	TOMMO_GENOMICS	ss5727675015	Oct 16, 2022 (156)
63	EVA	ss5823777015	Oct 16, 2022 (156)
64	EVA	ss5823777016	Oct 16, 2022 (156)
65	EVA	ss5823777017	Oct 16, 2022 (156)
66	1000Genomes	NC_000007.13 - 154232472	Oct 12, 2018 (152)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 281862777 (NC_000007.14:154535386::T 49586/137894) Row 281862778 (NC_000007.14:154535386::TT 50/138062) Row 281862780 (NC_000007.14:154535386:T: 37234/137982)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 281862777 (NC_000007.14:154535386::T 49586/137894) Row 281862778 (NC_000007.14:154535386::TT 50/138062) Row 281862780 (NC_000007.14:154535386:T: 37234/137982)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 281862777 (NC_000007.14:154535386::T 49586/137894) Row 281862778 (NC_000007.14:154535386::TT 50/138062) Row 281862780 (NC_000007.14:154535386:T: 37234/137982)...	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 281862777 (NC_000007.14:154535386::T 49586/137894) Row 281862778 (NC_000007.14:154535386::TT 50/138062) Row 281862780 (NC_000007.14:154535386:T: 37234/137982)...	-	Apr 26, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 281862777 (NC_000007.14:154535386::T 49586/137894) Row 281862778 (NC_000007.14:154535386::TT 50/138062) Row 281862780 (NC_000007.14:154535386:T: 37234/137982)...	-	Apr 26, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 281862777 (NC_000007.14:154535386::T 49586/137894) Row 281862778 (NC_000007.14:154535386::TT 50/138062) Row 281862780 (NC_000007.14:154535386:T: 37234/137982)...	-	Apr 26, 2021 (155)
73	Korean Genome Project Submission ignored due to conflicting rows: Row 19312583 (NC_000007.14:154535388::T 620/1832) Row 19312584 (NC_000007.14:154535387:T: 158/1832) Row 19312585 (NC_000007.14:154535386:TT: 124/1832)	-	Apr 26, 2020 (154)
74	Korean Genome Project Submission ignored due to conflicting rows: Row 19312583 (NC_000007.14:154535388::T 620/1832) Row 19312584 (NC_000007.14:154535387:T: 158/1832) Row 19312585 (NC_000007.14:154535386:TT: 124/1832)	-	Apr 26, 2020 (154)
75	Korean Genome Project Submission ignored due to conflicting rows: Row 19312583 (NC_000007.14:154535388::T 620/1832) Row 19312584 (NC_000007.14:154535387:T: 158/1832) Row 19312585 (NC_000007.14:154535386:TT: 124/1832)	-	Apr 26, 2020 (154)
76	8.3KJPN Submission ignored due to conflicting rows: Row 44386739 (NC_000007.13:154232471::T 6385/16758) Row 44386740 (NC_000007.13:154232471:T: 1063/16758) Row 44386741 (NC_000007.13:154232471:TT: 901/16758)...	-	Apr 26, 2021 (155)
77	8.3KJPN Submission ignored due to conflicting rows: Row 44386739 (NC_000007.13:154232471::T 6385/16758) Row 44386740 (NC_000007.13:154232471:T: 1063/16758) Row 44386741 (NC_000007.13:154232471:TT: 901/16758)...	-	Apr 26, 2021 (155)
78	8.3KJPN Submission ignored due to conflicting rows: Row 44386739 (NC_000007.13:154232471::T 6385/16758) Row 44386740 (NC_000007.13:154232471:T: 1063/16758) Row 44386741 (NC_000007.13:154232471:TT: 901/16758)...	-	Apr 26, 2021 (155)
79	8.3KJPN Submission ignored due to conflicting rows: Row 44386739 (NC_000007.13:154232471::T 6385/16758) Row 44386740 (NC_000007.13:154232471:T: 1063/16758) Row 44386741 (NC_000007.13:154232471:TT: 901/16758)...	-	Apr 26, 2021 (155)
80	14KJPN Submission ignored due to conflicting rows: Row 61512116 (NC_000007.14:154535386::T 10755/28258) Row 61512117 (NC_000007.14:154535386:T: 1785/28258) Row 61512118 (NC_000007.14:154535386:TT: 1484/28258)...	-	Oct 16, 2022 (156)
81	14KJPN Submission ignored due to conflicting rows: Row 61512116 (NC_000007.14:154535386::T 10755/28258) Row 61512117 (NC_000007.14:154535386:T: 1785/28258) Row 61512118 (NC_000007.14:154535386:TT: 1484/28258)...	-	Oct 16, 2022 (156)
82	14KJPN Submission ignored due to conflicting rows: Row 61512116 (NC_000007.14:154535386::T 10755/28258) Row 61512117 (NC_000007.14:154535386:T: 1785/28258) Row 61512118 (NC_000007.14:154535386:TT: 1484/28258)...	-	Oct 16, 2022 (156)
83	14KJPN Submission ignored due to conflicting rows: Row 61512116 (NC_000007.14:154535386::T 10755/28258) Row 61512117 (NC_000007.14:154535386:T: 1785/28258) Row 61512118 (NC_000007.14:154535386:TT: 1484/28258)...	-	Oct 16, 2022 (156)
84	ALFA	NC_000007.14 - 154535387	Apr 26, 2021 (155)

History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Associated ID	History Updated (Build)
rs138126731	May 11, 2012 (137)
rs143573339	May 11, 2012 (137)
rs201229251	May 15, 2013 (138)
rs796764319	Nov 08, 2017 (151)
rs35072938	May 11, 2012 (137)
rs58126970	May 11, 2012 (137)
rs72575639	May 13, 2013 (138)
rs72604749	Feb 27, 2009 (130)
rs143581841	May 04, 2012 (137)
rs869145766	Nov 08, 2017 (151)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4176235717, ss5275390734, ss5472183457	NC_000007.14:154535386:TTTT:	NC_000007.14:154535386:TTTTTTTTTTT… NC_000007.14:154535386:TTTTTTTTTTTT:TTTTTTTT	(self)
11050666151	NC_000007.14:154535386:TTTTTTTTTTT… NC_000007.14:154535386:TTTTTTTTTTTT:TTTTTTTT	NC_000007.14:154535386:TTTTTTTTTTT… NC_000007.14:154535386:TTTTTTTTTTTT:TTTTTTTT	(self)
ss4176235716, ss5275390735, ss5472183458	NC_000007.14:154535386:TTT:	NC_000007.14:154535386:TTTTTTTTTTT… NC_000007.14:154535386:TTTTTTTTTTTT:TTTTTTTTT	(self)
11050666151	NC_000007.14:154535386:TTTTTTTTTTT… NC_000007.14:154535386:TTTTTTTTTTTT:TTTTTTTTT	NC_000007.14:154535386:TTTTTTTTTTT… NC_000007.14:154535386:TTTTTTTTTTTT:TTTTTTTTT	(self)
ss295363852	NC_000007.12:153863404:TT:	NC_000007.14:154535386:TTTTTTTTTTT… NC_000007.14:154535386:TTTTTTTTTTTT:TTTTTTTTTT	(self)
ss295363854	NC_000007.12:153863414:TT:	NC_000007.14:154535386:TTTTTTTTTTT… NC_000007.14:154535386:TTTTTTTTTTTT:TTTTTTTTTT	(self)
ss3002346432, ss5186417434, ss5823777017	NC_000007.13:154232471:TT:	NC_000007.14:154535386:TTTTTTTTTTT… NC_000007.14:154535386:TTTTTTTTTTTT:TTTTTTTTTT	(self)
ss3066180097, ss3646068710, ss3721049271, ss3962934584, ss4176235715, ss5275390733, ss5472183454, ss5727675014	NC_000007.14:154535386:TT:	NC_000007.14:154535386:TTTTTTTTTTT… NC_000007.14:154535386:TTTTTTTTTTTT:TTTTTTTTTT	(self)
11050666151	NC_000007.14:154535386:TTTTTTTTTTT… NC_000007.14:154535386:TTTTTTTTTTTT:TTTTTTTTTT	NC_000007.14:154535386:TTTTTTTTTTT… NC_000007.14:154535386:TTTTTTTTTTTT:TTTTTTTTTT	(self)
ss95480412, ss98216373	NT_007914.15:14828104:TT:	NC_000007.14:154535386:TTTTTTTTTTT… NC_000007.14:154535386:TTTTTTTTTTTT:TTTTTTTTTT	(self)
ss79812677	NC_000007.11:153670130:T:	NC_000007.14:154535386:TTTTTTTTTTT… NC_000007.14:154535386:TTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss288882844	NC_000007.12:153863404:T:	NC_000007.14:154535386:TTTTTTTTTTT… NC_000007.14:154535386:TTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss666423281, ss3644252481, ss3830911600, ss5186417433, ss5823777016	NC_000007.13:154232471:T:	NC_000007.14:154535386:TTTTTTTTTTT… NC_000007.14:154535386:TTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss3646068709, ss4176235714, ss5275390731, ss5472183456, ss5727675013	NC_000007.14:154535386:T:	NC_000007.14:154535386:TTTTTTTTTTT… NC_000007.14:154535386:TTTTTTTTTTTT:TTTTTTTTTTT	(self)
11050666151	NC_000007.14:154535386:TTTTTTTTTTT… NC_000007.14:154535386:TTTTTTTTTTTT:TTTTTTTTTTT	NC_000007.14:154535386:TTTTTTTTTTT… NC_000007.14:154535386:TTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss3721049272, ss3962934583	NC_000007.14:154535387:T:	NC_000007.14:154535386:TTTTTTTTTTT… NC_000007.14:154535386:TTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss42927005, ss287823895	NT_007914.15:14828094:T:	NC_000007.14:154535386:TTTTTTTTTTT… NC_000007.14:154535386:TTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss42979961	NT_007914.15:14828095:T:	NC_000007.14:154535386:TTTTTTTTTTT… NC_000007.14:154535386:TTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss193955671	NT_007933.16:92028607:T:	NC_000007.14:154535386:TTTTTTTTTTT… NC_000007.14:154535386:TTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss295363853	NC_000007.12:153863410::T	NC_000007.14:154535386:TTTTTTTTTTT… NC_000007.14:154535386:TTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss288882845	NC_000007.12:153863416::T	NC_000007.14:154535386:TTTTTTTTTTT… NC_000007.14:154535386:TTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
39921796, ss663759858, ss1367796575, ss3786010107, ss3791281028, ss3796161369, ss5186417432, ss5823777015	NC_000007.13:154232471::T	NC_000007.14:154535386:TTTTTTTTTTT… NC_000007.14:154535386:TTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss3838957093	NC_000007.13:154232472::T	NC_000007.14:154535386:TTTTTTTTTTT… NC_000007.14:154535386:TTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss3810548900, ss4176235711, ss5275390732, ss5472183455, ss5727675012	NC_000007.14:154535386::T	NC_000007.14:154535386:TTTTTTTTTTT… NC_000007.14:154535386:TTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
11050666151	NC_000007.14:154535386:TTTTTTTTTTT… NC_000007.14:154535386:TTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000007.14:154535386:TTTTTTTTTTT… NC_000007.14:154535386:TTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss3844414851	NC_000007.14:154535387::T	NC_000007.14:154535386:TTTTTTTTTTT… NC_000007.14:154535386:TTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss3721049273, ss3962934582	NC_000007.14:154535388::T	NC_000007.14:154535386:TTTTTTTTTTT… NC_000007.14:154535386:TTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss42931638	NT_007914.15:14828096::T	NC_000007.14:154535386:TTTTTTTTTTT… NC_000007.14:154535386:TTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss98216373	NT_007914.15:14828104:TT:TTT	NC_000007.14:154535386:TTTTTTTTTTT… NC_000007.14:154535386:TTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss104781544, ss105539452	NT_007914.15:14828105::T	NC_000007.14:154535386:TTTTTTTTTTT… NC_000007.14:154535386:TTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss5186417435	NC_000007.13:154232471::TT	NC_000007.14:154535386:TTTTTTTTTTT… NC_000007.14:154535386:TTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4176235712, ss5275390736, ss5727675015	NC_000007.14:154535386::TT	NC_000007.14:154535386:TTTTTTTTTTT… NC_000007.14:154535386:TTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
11050666151	NC_000007.14:154535386:TTTTTTTTTTT… NC_000007.14:154535386:TTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000007.14:154535386:TTTTTTTTTTT… NC_000007.14:154535386:TTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss3721049274	NC_000007.14:154535388::TT	NC_000007.14:154535386:TTTTTTTTTTT… NC_000007.14:154535386:TTTTTTTTTTTT:TTTTTTTTTTTTTT	(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 rs34372202

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

rs34372202