Name: rs67181334
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.

rs67181334

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr7:117319523-117319533 (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: delGGG / delGG / delG / dupG / dup…
delGGG / delGG / delG / dupG / dupGG / dupGGG
Variation Type: Indel Insertion and Deletion
Frequency: delG=0.1855 (1819/9806, ALFA)
delG=0.45 (18/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: WNT2 : Intron Variant
LOC105375467 : 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	9806	GGGGGGGGGGG=0.8084	GGGGGGGGG=0.0011, GGGGGGGGGG=0.1855, GGGGGGGGGGGG=0.0048, GGGGGGGGGGGGG=0.0002, GGGGGGGGGGGGGG=0.0000	0.713666	0.084228	0.202106	32
European	Sub	7962	GGGGGGGGGGG=0.7644	GGGGGGGGG=0.0014, GGGGGGGGGG=0.2281, GGGGGGGGGGGG=0.0059, GGGGGGGGGGGGG=0.0003, GGGGGGGGGGGGGG=0.0000	0.647119	0.104029	0.248853	32
African	Sub	1104	GGGGGGGGGGG=1.0000	GGGGGGGGG=0.0000, GGGGGGGGGG=0.0000, GGGGGGGGGGGG=0.0000, GGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGG=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	36	GGGGGGGGGGG=1.00	GGGGGGGGG=0.00, GGGGGGGGGG=0.00, GGGGGGGGGGGG=0.00, GGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGG=0.00	1.0	0.0	0.0	N/A
African American	Sub	1068	GGGGGGGGGGG=1.0000	GGGGGGGGG=0.0000, GGGGGGGGGG=0.0000, GGGGGGGGGGGG=0.0000, GGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGG=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	94	GGGGGGGGGGG=1.00	GGGGGGGGG=0.00, GGGGGGGGGG=0.00, GGGGGGGGGGGG=0.00, GGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGG=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	74	GGGGGGGGGGG=1.00	GGGGGGGGG=0.00, GGGGGGGGGG=0.00, GGGGGGGGGGGG=0.00, GGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGG=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	20	GGGGGGGGGGG=1.00	GGGGGGGGG=0.00, GGGGGGGGGG=0.00, GGGGGGGGGGGG=0.00, GGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGG=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	70	GGGGGGGGGGG=1.00	GGGGGGGGG=0.00, GGGGGGGGGG=0.00, GGGGGGGGGGGG=0.00, GGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGG=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	308	GGGGGGGGGGG=1.000	GGGGGGGGG=0.000, GGGGGGGGGG=0.000, GGGGGGGGGGGG=0.000, GGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGG=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	38	GGGGGGGGGGG=1.00	GGGGGGGGG=0.00, GGGGGGGGGG=0.00, GGGGGGGGGGGG=0.00, GGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGG=0.00	1.0	0.0	0.0	N/A
Other	Sub	230	GGGGGGGGGGG=0.987	GGGGGGGGG=0.000, GGGGGGGGGG=0.013, GGGGGGGGGGGG=0.000, GGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGG=0.000	0.973913	0.0	0.026087	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	9806	(G)₁₁=0.8084	delGG=0.0011, delG=0.1855, dupG=0.0048, dupGG=0.0002, dupGGG=0.0000
Allele Frequency Aggregator	European	Sub	7962	(G)₁₁=0.7644	delGG=0.0014, delG=0.2281, dupG=0.0059, dupGG=0.0003, dupGGG=0.0000
Allele Frequency Aggregator	African	Sub	1104	(G)₁₁=1.0000	delGG=0.0000, delG=0.0000, dupG=0.0000, dupGG=0.0000, dupGGG=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	308	(G)₁₁=1.000	delGG=0.000, delG=0.000, dupG=0.000, dupGG=0.000, dupGGG=0.000
Allele Frequency Aggregator	Other	Sub	230	(G)₁₁=0.987	delGG=0.000, delG=0.013, dupG=0.000, dupGG=0.000, dupGGG=0.000
Allele Frequency Aggregator	Asian	Sub	94	(G)₁₁=1.00	delGG=0.00, delG=0.00, dupG=0.00, dupGG=0.00, dupGGG=0.00
Allele Frequency Aggregator	Latin American 1	Sub	70	(G)₁₁=1.00	delGG=0.00, delG=0.00, dupG=0.00, dupGG=0.00, dupGGG=0.00
Allele Frequency Aggregator	South Asian	Sub	38	(G)₁₁=1.00	delGG=0.00, delG=0.00, dupG=0.00, dupGG=0.00, dupGGG=0.00
The Danish reference pan genome	Danish	Study-wide	40	(G)₁₁=0.55	delG=0.45

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.117319531_117319533del
GRCh38.p14 chr 7	NC_000007.14:g.117319532_117319533del
GRCh38.p14 chr 7	NC_000007.14:g.117319533del
GRCh38.p14 chr 7	NC_000007.14:g.117319533dup
GRCh38.p14 chr 7	NC_000007.14:g.117319532_117319533dup
GRCh38.p14 chr 7	NC_000007.14:g.117319531_117319533dup
GRCh37.p13 chr 7	NC_000007.13:g.116959585_116959587del
GRCh37.p13 chr 7	NC_000007.13:g.116959586_116959587del
GRCh37.p13 chr 7	NC_000007.13:g.116959587del
GRCh37.p13 chr 7	NC_000007.13:g.116959587dup
GRCh37.p13 chr 7	NC_000007.13:g.116959586_116959587dup
GRCh37.p13 chr 7	NC_000007.13:g.116959585_116959587dup

Gene: WNT2, Wnt family member 2 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
WNT2 transcript variant 1	NM_003391.3:c.310+1042_31… NM_003391.3:c.310+1042_310+1044del	N/A	Intron Variant
WNT2 transcript variant 2	NR_024047.2:n.	N/A	Intron Variant

Gene: LOC105375467, uncharacterized LOC105375467 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LOC105375467 transcript	XR_007060645.1: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	(G)₁₁=	delGGG	delGG	delG	dupG	dupGG	dupGGG
GRCh38.p14 chr 7	NC_000007.14:g.117319523_117319533=	NC_000007.14:g.117319531_117319533del	NC_000007.14:g.117319532_117319533del	NC_000007.14:g.117319533del	NC_000007.14:g.117319533dup	NC_000007.14:g.117319532_117319533dup	NC_000007.14:g.117319531_117319533dup
GRCh37.p13 chr 7	NC_000007.13:g.116959577_116959587=	NC_000007.13:g.116959585_116959587del	NC_000007.13:g.116959586_116959587del	NC_000007.13:g.116959587del	NC_000007.13:g.116959587dup	NC_000007.13:g.116959586_116959587dup	NC_000007.13:g.116959585_116959587dup
WNT2 transcript variant 1	NM_003391.2:c.310+1044=	NM_003391.2:c.310+1042_310+1044del	NM_003391.2:c.310+1043_310+1044del	NM_003391.2:c.310+1044del	NM_003391.2:c.310+1044dup	NM_003391.2:c.310+1043_310+1044dup	NM_003391.2:c.310+1042_310+1044dup
WNT2 transcript variant 1	NM_003391.3:c.310+1044=	NM_003391.3:c.310+1042_310+1044del	NM_003391.3:c.310+1043_310+1044del	NM_003391.3:c.310+1044del	NM_003391.3:c.310+1044dup	NM_003391.3:c.310+1043_310+1044dup	NM_003391.3:c.310+1042_310+1044dup
WNT2 transcript variant X1	XM_005250563.1:c.86+1044=	XM_005250563.1:c.86+1042_86+1044del	XM_005250563.1:c.86+1043_86+1044del	XM_005250563.1:c.86+1044del	XM_005250563.1:c.86+1044dup	XM_005250563.1:c.86+1043_86+1044dup	XM_005250563.1:c.86+1042_86+1044dup

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#.

42 SubSNP, 19 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	BUSHMAN	ss193941759	Jul 04, 2010 (132)
2	GMI	ss287819269	May 09, 2011 (137)
3	EVA_GENOME_DK	ss1577074288	Apr 01, 2015 (144)
4	HAMMER_LAB	ss1805184825	Sep 08, 2015 (146)
5	SYSTEMSBIOZJU	ss2626824905	Nov 08, 2017 (151)
6	SWEGEN	ss3001907684	Nov 08, 2017 (151)
7	MCHAISSO	ss3065155058	Jan 10, 2018 (151)
8	EVA_DECODE	ss3720538314	Jul 13, 2019 (153)
9	EVA_DECODE	ss3720538315	Jul 13, 2019 (153)
10	EVA_DECODE	ss3720538316	Jul 13, 2019 (153)
11	EVA_DECODE	ss3720538317	Jul 13, 2019 (153)
12	ACPOP	ss3735002970	Jul 13, 2019 (153)
13	ACPOP	ss3735002971	Jul 13, 2019 (153)
14	ACPOP	ss3735002972	Jul 13, 2019 (153)
15	PACBIO	ss3785937163	Jul 13, 2019 (153)
16	PACBIO	ss3791219349	Jul 13, 2019 (153)
17	PACBIO	ss3796099469	Jul 13, 2019 (153)
18	EVA	ss3830780299	Apr 26, 2020 (154)
19	EVA	ss3838889257	Apr 26, 2020 (154)
20	EVA	ss3844345262	Apr 26, 2020 (154)
21	GNOMAD	ss4171620902	Apr 26, 2021 (155)
22	GNOMAD	ss4171620903	Apr 26, 2021 (155)
23	GNOMAD	ss4171620904	Apr 26, 2021 (155)
24	GNOMAD	ss4171620905	Apr 26, 2021 (155)
25	GNOMAD	ss4171620906	Apr 26, 2021 (155)
26	GNOMAD	ss4171620907	Apr 26, 2021 (155)
27	TOMMO_GENOMICS	ss5185228591	Apr 26, 2021 (155)
28	TOMMO_GENOMICS	ss5185228592	Apr 26, 2021 (155)
29	TOMMO_GENOMICS	ss5185228593	Apr 26, 2021 (155)
30	TOMMO_GENOMICS	ss5185228594	Apr 26, 2021 (155)
31	1000G_HIGH_COVERAGE	ss5274462444	Oct 13, 2022 (156)
32	1000G_HIGH_COVERAGE	ss5274462445	Oct 13, 2022 (156)
33	1000G_HIGH_COVERAGE	ss5274462446	Oct 13, 2022 (156)
34	HUGCELL_USP	ss5471376831	Oct 13, 2022 (156)
35	HUGCELL_USP	ss5471376832	Oct 13, 2022 (156)
36	HUGCELL_USP	ss5471376833	Oct 13, 2022 (156)
37	HUGCELL_USP	ss5471376834	Oct 13, 2022 (156)
38	TOMMO_GENOMICS	ss5726118179	Oct 13, 2022 (156)
39	TOMMO_GENOMICS	ss5726118180	Oct 13, 2022 (156)
40	TOMMO_GENOMICS	ss5726118181	Oct 13, 2022 (156)
41	TOMMO_GENOMICS	ss5726118182	Oct 13, 2022 (156)
42	EVA	ss5860566975	Oct 13, 2022 (156)
43	The Danish reference pan genome	NC_000007.13 - 116959577	Apr 26, 2020 (154)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 274293392 (NC_000007.14:117319522::G 4988/113298) Row 274293393 (NC_000007.14:117319522::GG 132/113646) Row 274293394 (NC_000007.14:117319522::GGG 8/113672)...	-	Apr 26, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 274293392 (NC_000007.14:117319522::G 4988/113298) Row 274293393 (NC_000007.14:117319522::GG 132/113646) Row 274293394 (NC_000007.14:117319522::GGG 8/113672)...	-	Apr 26, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 274293392 (NC_000007.14:117319522::G 4988/113298) Row 274293393 (NC_000007.14:117319522::GG 132/113646) Row 274293394 (NC_000007.14:117319522::GGG 8/113672)...	-	Apr 26, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 274293392 (NC_000007.14:117319522::G 4988/113298) Row 274293393 (NC_000007.14:117319522::GG 132/113646) Row 274293394 (NC_000007.14:117319522::GGG 8/113672)...	-	Apr 26, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 274293392 (NC_000007.14:117319522::G 4988/113298) Row 274293393 (NC_000007.14:117319522::GG 132/113646) Row 274293394 (NC_000007.14:117319522::GGG 8/113672)...	-	Apr 26, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 274293392 (NC_000007.14:117319522::G 4988/113298) Row 274293393 (NC_000007.14:117319522::GG 132/113646) Row 274293394 (NC_000007.14:117319522::GGG 8/113672)...	-	Apr 26, 2021 (155)
50	Northern Sweden Submission ignored due to conflicting rows: Row 8287835 (NC_000007.13:116959576:G: 221/600) Row 8287836 (NC_000007.13:116959576::G 16/600) Row 8287837 (NC_000007.13:116959576:GGG: 2/600)	-	Jul 13, 2019 (153)
51	Northern Sweden Submission ignored due to conflicting rows: Row 8287835 (NC_000007.13:116959576:G: 221/600) Row 8287836 (NC_000007.13:116959576::G 16/600) Row 8287837 (NC_000007.13:116959576:GGG: 2/600)	-	Jul 13, 2019 (153)
52	Northern Sweden Submission ignored due to conflicting rows: Row 8287835 (NC_000007.13:116959576:G: 221/600) Row 8287836 (NC_000007.13:116959576::G 16/600) Row 8287837 (NC_000007.13:116959576:GGG: 2/600)	-	Jul 13, 2019 (153)
53	8.3KJPN Submission ignored due to conflicting rows: Row 43197898 (NC_000007.13:116959576:G: 920/16750) Row 43197899 (NC_000007.13:116959576::G 149/16750) Row 43197900 (NC_000007.13:116959576::GG 8/16750)...	-	Apr 26, 2021 (155)
54	8.3KJPN Submission ignored due to conflicting rows: Row 43197898 (NC_000007.13:116959576:G: 920/16750) Row 43197899 (NC_000007.13:116959576::G 149/16750) Row 43197900 (NC_000007.13:116959576::GG 8/16750)...	-	Apr 26, 2021 (155)
55	8.3KJPN Submission ignored due to conflicting rows: Row 43197898 (NC_000007.13:116959576:G: 920/16750) Row 43197899 (NC_000007.13:116959576::G 149/16750) Row 43197900 (NC_000007.13:116959576::GG 8/16750)...	-	Apr 26, 2021 (155)
56	8.3KJPN Submission ignored due to conflicting rows: Row 43197898 (NC_000007.13:116959576:G: 920/16750) Row 43197899 (NC_000007.13:116959576::G 149/16750) Row 43197900 (NC_000007.13:116959576::GG 8/16750)...	-	Apr 26, 2021 (155)
57	14KJPN Submission ignored due to conflicting rows: Row 59955283 (NC_000007.14:117319522:G: 1473/28246) Row 59955284 (NC_000007.14:117319522::G 277/28246) Row 59955285 (NC_000007.14:117319522::GG 17/28246)...	-	Oct 13, 2022 (156)
58	14KJPN Submission ignored due to conflicting rows: Row 59955283 (NC_000007.14:117319522:G: 1473/28246) Row 59955284 (NC_000007.14:117319522::G 277/28246) Row 59955285 (NC_000007.14:117319522::GG 17/28246)...	-	Oct 13, 2022 (156)
59	14KJPN Submission ignored due to conflicting rows: Row 59955283 (NC_000007.14:117319522:G: 1473/28246) Row 59955284 (NC_000007.14:117319522::G 277/28246) Row 59955285 (NC_000007.14:117319522::GG 17/28246)...	-	Oct 13, 2022 (156)
60	14KJPN Submission ignored due to conflicting rows: Row 59955283 (NC_000007.14:117319522:G: 1473/28246) Row 59955284 (NC_000007.14:117319522::G 277/28246) Row 59955285 (NC_000007.14:117319522::GG 17/28246)...	-	Oct 13, 2022 (156)
61	ALFA	NC_000007.14 - 117319523	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)
rs67181335	Feb 26, 2009 (130)
rs143934368	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss3001907684, ss3735002972	NC_000007.13:116959576:GGG:	NC_000007.14:117319522:GGGGGGGGGGG… NC_000007.14:117319522:GGGGGGGGGGG:GGGGGGGG	(self)
ss3720538317, ss4171620907, ss5471376834	NC_000007.14:117319522:GGG:	NC_000007.14:117319522:GGGGGGGGGGG… NC_000007.14:117319522:GGGGGGGGGGG:GGGGGGGG	(self)
ss5185228594	NC_000007.13:116959576:GG:	NC_000007.14:117319522:GGGGGGGGGGG… NC_000007.14:117319522:GGGGGGGGGGG:GGGGGGGGG	(self)
ss3065155058, ss4171620906, ss5726118182	NC_000007.14:117319522:GG:	NC_000007.14:117319522:GGGGGGGGGGG… NC_000007.14:117319522:GGGGGGGGGGG:GGGGGGGGG	(self)
4611491958	NC_000007.14:117319522:GGGGGGGGGGG… NC_000007.14:117319522:GGGGGGGGGGG:GGGGGGGGG	NC_000007.14:117319522:GGGGGGGGGGG… NC_000007.14:117319522:GGGGGGGGGGG:GGGGGGGGG	(self)
ss3720538316	NC_000007.14:117319523:GG:	NC_000007.14:117319522:GGGGGGGGGGG… NC_000007.14:117319522:GGGGGGGGGGG:GGGGGGGGG	(self)
1178675, ss1577074288, ss1805184825, ss2626824905, ss3735002970, ss3785937163, ss3791219349, ss3796099469, ss3830780299, ss3838889257, ss5185228591	NC_000007.13:116959576:G:	NC_000007.14:117319522:GGGGGGGGGGG… NC_000007.14:117319522:GGGGGGGGGGG:GGGGGGGGGG	(self)
ss3844345262, ss4171620905, ss5274462445, ss5471376831, ss5726118179, ss5860566975	NC_000007.14:117319522:G:	NC_000007.14:117319522:GGGGGGGGGGG… NC_000007.14:117319522:GGGGGGGGGGG:GGGGGGGGGG	(self)
4611491958	NC_000007.14:117319522:GGGGGGGGGGG… NC_000007.14:117319522:GGGGGGGGGGG:GGGGGGGGGG	NC_000007.14:117319522:GGGGGGGGGGG… NC_000007.14:117319522:GGGGGGGGGGG:GGGGGGGGGG	(self)
ss3720538315	NC_000007.14:117319524:G:	NC_000007.14:117319522:GGGGGGGGGGG… NC_000007.14:117319522:GGGGGGGGGGG:GGGGGGGGGG	(self)
ss287819269	NT_007933.15:54992419:G:	NC_000007.14:117319522:GGGGGGGGGGG… NC_000007.14:117319522:GGGGGGGGGGG:GGGGGGGGGG	(self)
ss3735002971, ss5185228592	NC_000007.13:116959576::G	NC_000007.14:117319522:GGGGGGGGGGG… NC_000007.14:117319522:GGGGGGGGGGG:GGGGGGGGGGGG	(self)
ss4171620902, ss5274462444, ss5471376832, ss5726118180	NC_000007.14:117319522::G	NC_000007.14:117319522:GGGGGGGGGGG… NC_000007.14:117319522:GGGGGGGGGGG:GGGGGGGGGGGG	(self)
4611491958	NC_000007.14:117319522:GGGGGGGGGGG… NC_000007.14:117319522:GGGGGGGGGGG:GGGGGGGGGGGG	NC_000007.14:117319522:GGGGGGGGGGG… NC_000007.14:117319522:GGGGGGGGGGG:GGGGGGGGGGGG	(self)
ss3720538314	NC_000007.14:117319525::G	NC_000007.14:117319522:GGGGGGGGGGG… NC_000007.14:117319522:GGGGGGGGGGG:GGGGGGGGGGGG	(self)
ss193941759	NT_007933.16:54812743::G	NC_000007.14:117319522:GGGGGGGGGGG… NC_000007.14:117319522:GGGGGGGGGGG:GGGGGGGGGGGG	(self)
ss5185228593	NC_000007.13:116959576::GG	NC_000007.14:117319522:GGGGGGGGGGG… NC_000007.14:117319522:GGGGGGGGGGG:GGGGGGGGGGGGG	(self)
ss4171620903, ss5274462446, ss5471376833, ss5726118181	NC_000007.14:117319522::GG	NC_000007.14:117319522:GGGGGGGGGGG… NC_000007.14:117319522:GGGGGGGGGGG:GGGGGGGGGGGGG	(self)
4611491958	NC_000007.14:117319522:GGGGGGGGGGG… NC_000007.14:117319522:GGGGGGGGGGG:GGGGGGGGGGGGG	NC_000007.14:117319522:GGGGGGGGGGG… NC_000007.14:117319522:GGGGGGGGGGG:GGGGGGGGGGGGG	(self)
ss4171620904	NC_000007.14:117319522::GGG	NC_000007.14:117319522:GGGGGGGGGGG… NC_000007.14:117319522:GGGGGGGGGGG:GGGGGGGGGGGGGG	(self)
4611491958	NC_000007.14:117319522:GGGGGGGGGGG… NC_000007.14:117319522:GGGGGGGGGGG:GGGGGGGGGGGGGG	NC_000007.14:117319522:GGGGGGGGGGG… NC_000007.14:117319522:GGGGGGGGGGG:GGGGGGGGGGGGGG	(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 rs67181334

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
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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

rs67181334