Name: rs63137960
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.

rs63137960

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr12:56205570-56205579 (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: delGG / delG / dupG / dupGG / dupG…
delGG / delG / dupG / dupGG / dupGGG / dup(G)₄ / dup(G)₅
Variation Type: Indel Insertion and Deletion
Frequency: delGG=0.0000 (0/9354, ALFA)
delG=0.0000 (0/9354, ALFA)
dupG=0.0000 (0/9354, ALFA) (+ 9 more)
dupGG=0.0000 (0/9354, ALFA)
dupGGG=0.0000 (0/9354, ALFA)
dup(G)₄=0.0000 (0/9354, ALFA)
dup(G)₅=0.0000 (0/9354, ALFA)
dupG=0.0843 (422/5008, 1000G)
dupG=0.0979 (433/4422, Estonian)
dupG=0.0727 (280/3854, ALSPAC)
dupG=0.0666 (247/3708, TWINSUK)
dupG=0.10 (4/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: RNF41 : Non Coding Transcript 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	9354	GGGGGGGGGG=1.0000	GGGGGGGG=0.0000, GGGGGGGGG=0.0000, GGGGGGGGGGG=0.0000, GGGGGGGGGGGG=0.0000, GGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGGG=0.0000	1.0	N/A
European	Sub	6052	GGGGGGGGGG=1.0000	GGGGGGGG=0.0000, GGGGGGGGG=0.0000, GGGGGGGGGGG=0.0000, GGGGGGGGGGGG=0.0000, GGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGGG=0.0000	1.0	N/A
African	Sub	2140	GGGGGGGGGG=1.0000	GGGGGGGG=0.0000, GGGGGGGGG=0.0000, GGGGGGGGGGG=0.0000, GGGGGGGGGGGG=0.0000, GGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGGG=0.0000	1.0	N/A
African Others	Sub	78	GGGGGGGGGG=1.00	GGGGGGGG=0.00, GGGGGGGGG=0.00, GGGGGGGGGGG=0.00, GGGGGGGGGGGG=0.00, GGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGG=0.00	1.0	N/A
African American	Sub	2062	GGGGGGGGGG=1.0000	GGGGGGGG=0.0000, GGGGGGGGG=0.0000, GGGGGGGGGGG=0.0000, GGGGGGGGGGGG=0.0000, GGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGGG=0.0000	1.0	N/A
Asian	Sub	100	GGGGGGGGGG=1.00	GGGGGGGG=0.00, GGGGGGGGG=0.00, GGGGGGGGGGG=0.00, GGGGGGGGGGGG=0.00, GGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGG=0.00	1.0	N/A
East Asian	Sub	76	GGGGGGGGGG=1.00	GGGGGGGG=0.00, GGGGGGGGG=0.00, GGGGGGGGGGG=0.00, GGGGGGGGGGGG=0.00, GGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGG=0.00	1.0	N/A
Other Asian	Sub	24	GGGGGGGGGG=1.00	GGGGGGGG=0.00, GGGGGGGGG=0.00, GGGGGGGGGGG=0.00, GGGGGGGGGGGG=0.00, GGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGG=0.00	1.0	N/A
Latin American 1	Sub	102	GGGGGGGGGG=1.000	GGGGGGGG=0.000, GGGGGGGGG=0.000, GGGGGGGGGGG=0.000, GGGGGGGGGGGG=0.000, GGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGG=0.000	1.0	N/A
Latin American 2	Sub	526	GGGGGGGGGG=1.000	GGGGGGGG=0.000, GGGGGGGGG=0.000, GGGGGGGGGGG=0.000, GGGGGGGGGGGG=0.000, GGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGG=0.000	1.0	N/A
South Asian	Sub	72	GGGGGGGGGG=1.00	GGGGGGGG=0.00, GGGGGGGGG=0.00, GGGGGGGGGGG=0.00, GGGGGGGGGGGG=0.00, GGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGG=0.00	1.0	N/A
Other	Sub	362	GGGGGGGGGG=1.000	GGGGGGGG=0.000, GGGGGGGGG=0.000, GGGGGGGGGGG=0.000, GGGGGGGGGGGG=0.000, GGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGG=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	9354	(G)₁₀=1.0000	delGG=0.0000, delG=0.0000, dupG=0.0000, dupGG=0.0000, dupGGG=0.0000, dup(G)₄=0.0000, dup(G)₅=0.0000
Allele Frequency Aggregator	European	Sub	6052	(G)₁₀=1.0000	delGG=0.0000, delG=0.0000, dupG=0.0000, dupGG=0.0000, dupGGG=0.0000, dup(G)₄=0.0000, dup(G)₅=0.0000
Allele Frequency Aggregator	African	Sub	2140	(G)₁₀=1.0000	delGG=0.0000, delG=0.0000, dupG=0.0000, dupGG=0.0000, dupGGG=0.0000, dup(G)₄=0.0000, dup(G)₅=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	526	(G)₁₀=1.000	delGG=0.000, delG=0.000, dupG=0.000, dupGG=0.000, dupGGG=0.000, dup(G)₄=0.000, dup(G)₅=0.000
Allele Frequency Aggregator	Other	Sub	362	(G)₁₀=1.000	delGG=0.000, delG=0.000, dupG=0.000, dupGG=0.000, dupGGG=0.000, dup(G)₄=0.000, dup(G)₅=0.000
Allele Frequency Aggregator	Latin American 1	Sub	102	(G)₁₀=1.000	delGG=0.000, delG=0.000, dupG=0.000, dupGG=0.000, dupGGG=0.000, dup(G)₄=0.000, dup(G)₅=0.000
Allele Frequency Aggregator	Asian	Sub	100	(G)₁₀=1.00	delGG=0.00, delG=0.00, dupG=0.00, dupGG=0.00, dupGGG=0.00, dup(G)₄=0.00, dup(G)₅=0.00
Allele Frequency Aggregator	South Asian	Sub	72	(G)₁₀=1.00	delGG=0.00, delG=0.00, dupG=0.00, dupGG=0.00, dupGGG=0.00, dup(G)₄=0.00, dup(G)₅=0.00
1000Genomes	Global	Study-wide	5008	- No frequency provided	dupG=0.0843
1000Genomes	African	Sub	1322	- No frequency provided	dupG=0.1059
1000Genomes	East Asian	Sub	1008	- No frequency provided	dupG=0.0347
1000Genomes	Europe	Sub	1006	- No frequency provided	dupG=0.1173
1000Genomes	South Asian	Sub	978	- No frequency provided	dupG=0.079
1000Genomes	American	Sub	694	- No frequency provided	dupG=0.075
Genetic variation in the Estonian population	Estonian	Study-wide	4422	- No frequency provided	dupG=0.0979
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	- No frequency provided	dupG=0.0727
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	- No frequency provided	dupG=0.0666
The Danish reference pan genome	Danish	Study-wide	40	- No frequency provided	dupG=0.10

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 12	NC_000012.12:g.56205578_56205579del
GRCh38.p14 chr 12	NC_000012.12:g.56205579del
GRCh38.p14 chr 12	NC_000012.12:g.56205579dup
GRCh38.p14 chr 12	NC_000012.12:g.56205578_56205579dup
GRCh38.p14 chr 12	NC_000012.12:g.56205577_56205579dup
GRCh38.p14 chr 12	NC_000012.12:g.56205576_56205579dup
GRCh38.p14 chr 12	NC_000012.12:g.56205575_56205579dup
GRCh37.p13 chr 12	NC_000012.11:g.56599362_56599363del
GRCh37.p13 chr 12	NC_000012.11:g.56599363del
GRCh37.p13 chr 12	NC_000012.11:g.56599363dup
GRCh37.p13 chr 12	NC_000012.11:g.56599362_56599363dup
GRCh37.p13 chr 12	NC_000012.11:g.56599361_56599363dup
GRCh37.p13 chr 12	NC_000012.11:g.56599360_56599363dup
GRCh37.p13 chr 12	NC_000012.11:g.56599359_56599363dup

Gene: RNF41, ring finger protein 41 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
RNF41 transcript variant 3	NM_194359.2:c.868_877=	N/A	3 Prime UTR Variant
RNF41 transcript variant 1	NM_005785.4:c.868_877=	N/A	3 Prime UTR Variant
RNF41 transcript variant 2	NM_194358.3:c.868_877=	N/A	3 Prime UTR Variant
RNF41 transcript variant 4	NM_001242826.2:c.868_87… NM_001242826.2:c.868_877=	N/A	3 Prime UTR Variant
RNF41 transcript variant 5	NR_040053.2:n.2487_2488del	N/A	Non Coding Transcript Variant
RNF41 transcript variant 5	NR_040053.2:n.2488del	N/A	Non Coding Transcript Variant
RNF41 transcript variant 5	NR_040053.2:n.2488dup	N/A	Non Coding Transcript Variant
RNF41 transcript variant 5	NR_040053.2:n.2487_2488dup	N/A	Non Coding Transcript Variant
RNF41 transcript variant 5	NR_040053.2:n.2486_2488dup	N/A	Non Coding Transcript Variant
RNF41 transcript variant 5	NR_040053.2:n.2485_2488dup	N/A	Non Coding Transcript Variant
RNF41 transcript variant 5	NR_040053.2:n.2484_2488dup	N/A	Non Coding Transcript Variant
RNF41 transcript variant X1	XM_047428054.1:c.	N/A	Genic Downstream 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	(G)₁₀=	delGG	delG	dupG	dupGG	dupGGG	dup(G)₄	dup(G)₅
GRCh38.p14 chr 12	NC_000012.12:g.56205570_56205579=	NC_000012.12:g.56205578_56205579del	NC_000012.12:g.56205579del	NC_000012.12:g.56205579dup	NC_000012.12:g.56205578_56205579dup	NC_000012.12:g.56205577_56205579dup	NC_000012.12:g.56205576_56205579dup	NC_000012.12:g.56205575_56205579dup
GRCh37.p13 chr 12	NC_000012.11:g.56599354_56599363=	NC_000012.11:g.56599362_56599363del	NC_000012.11:g.56599363del	NC_000012.11:g.56599363dup	NC_000012.11:g.56599362_56599363dup	NC_000012.11:g.56599361_56599363dup	NC_000012.11:g.56599360_56599363dup	NC_000012.11:g.56599359_56599363dup
RNF41 transcript variant 1	NM_005785.4:c.868_877=	NM_005785.4:c.876_877del	NM_005785.4:c.*877del	NM_005785.4:c.*877dup	NM_005785.4:c.876_877dup	NM_005785.4:c.875_877dup	NM_005785.4:c.874_877dup	NM_005785.4:c.873_877dup
RNF41 transcript variant 1	NM_005785.3:c.868_877=	NM_005785.3:c.876_877del	NM_005785.3:c.*877del	NM_005785.3:c.*877dup	NM_005785.3:c.876_877dup	NM_005785.3:c.875_877dup	NM_005785.3:c.874_877dup	NM_005785.3:c.873_877dup
RNF41 transcript variant 2	NM_194358.3:c.868_877=	NM_194358.3:c.876_877del	NM_194358.3:c.*877del	NM_194358.3:c.*877dup	NM_194358.3:c.876_877dup	NM_194358.3:c.875_877dup	NM_194358.3:c.874_877dup	NM_194358.3:c.873_877dup
RNF41 transcript variant 2	NM_194358.2:c.868_877=	NM_194358.2:c.876_877del	NM_194358.2:c.*877del	NM_194358.2:c.*877dup	NM_194358.2:c.876_877dup	NM_194358.2:c.875_877dup	NM_194358.2:c.874_877dup	NM_194358.2:c.873_877dup
RNF41 transcript variant 5	NR_040053.2:n.2479_2488=	NR_040053.2:n.2487_2488del	NR_040053.2:n.2488del	NR_040053.2:n.2488dup	NR_040053.2:n.2487_2488dup	NR_040053.2:n.2486_2488dup	NR_040053.2:n.2485_2488dup	NR_040053.2:n.2484_2488dup
RNF41 transcript variant 5	NR_040053.1:n.2488_2497=	NR_040053.1:n.2496_2497del	NR_040053.1:n.2497del	NR_040053.1:n.2497dup	NR_040053.1:n.2496_2497dup	NR_040053.1:n.2495_2497dup	NR_040053.1:n.2494_2497dup	NR_040053.1:n.2493_2497dup
RNF41 transcript variant 4	NM_001242826.2:c.868_877=	NM_001242826.2:c.876_877del	NM_001242826.2:c.*877del	NM_001242826.2:c.*877dup	NM_001242826.2:c.876_877dup	NM_001242826.2:c.875_877dup	NM_001242826.2:c.874_877dup	NM_001242826.2:c.873_877dup
RNF41 transcript variant 4	NM_001242826.1:c.868_877=	NM_001242826.1:c.876_877del	NM_001242826.1:c.*877del	NM_001242826.1:c.*877dup	NM_001242826.1:c.876_877dup	NM_001242826.1:c.875_877dup	NM_001242826.1:c.874_877dup	NM_001242826.1:c.873_877dup
RNF41 transcript variant 3	NM_194359.2:c.868_877=	NM_194359.2:c.876_877del	NM_194359.2:c.*877del	NM_194359.2:c.*877dup	NM_194359.2:c.876_877dup	NM_194359.2:c.875_877dup	NM_194359.2:c.874_877dup	NM_194359.2:c.873_877dup

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#.

43 SubSNP, 20 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HUMANGENOME_JCVI	ss97271803	Feb 13, 2009 (130)
2	PJP	ss294753917	May 09, 2011 (137)
3	1000GENOMES	ss499756472	May 04, 2012 (137)
4	LUNTER	ss552218392	Apr 25, 2013 (138)
5	1000GENOMES	ss1372202446	Aug 21, 2014 (142)
6	EVA_GENOME_DK	ss1574507344	Apr 01, 2015 (144)
7	EVA_UK10K_ALSPAC	ss1707479222	Apr 01, 2015 (144)
8	EVA_UK10K_TWINSUK	ss1707479359	Apr 01, 2015 (144)
9	TMC_SNPDB	ss1997053066	Jul 19, 2016 (147)
10	BIOINF_KMB_FNS_UNIBA	ss3645254578	Oct 12, 2018 (152)
11	URBANLAB	ss3649844410	Oct 12, 2018 (152)
12	EGCUT_WGS	ss3677012035	Jul 13, 2019 (153)
13	EVA_DECODE	ss3693733931	Jul 13, 2019 (153)
14	EVA_DECODE	ss3693733932	Jul 13, 2019 (153)
15	EVA_DECODE	ss3693733933	Jul 13, 2019 (153)
16	ACPOP	ss3739050052	Jul 13, 2019 (153)
17	ACPOP	ss3739050053	Jul 13, 2019 (153)
18	PACBIO	ss3787235480	Jul 13, 2019 (153)
19	PACBIO	ss3792335458	Jul 13, 2019 (153)
20	PACBIO	ss3797218225	Jul 13, 2019 (153)
21	KHV_HUMAN_GENOMES	ss3815848988	Jul 13, 2019 (153)
22	EVA	ss3833139423	Apr 27, 2020 (154)
23	EVA	ss3986059999	Apr 26, 2021 (155)
24	GNOMAD	ss4252372053	Apr 26, 2021 (155)
25	GNOMAD	ss4252372054	Apr 26, 2021 (155)
26	GNOMAD	ss4252372055	Apr 26, 2021 (155)
27	GNOMAD	ss4252372056	Apr 26, 2021 (155)
28	GNOMAD	ss4252372057	Apr 26, 2021 (155)
29	GNOMAD	ss4252372058	Apr 26, 2021 (155)
30	TOMMO_GENOMICS	ss5206473930	Apr 26, 2021 (155)
31	TOMMO_GENOMICS	ss5206473931	Apr 26, 2021 (155)
32	TOMMO_GENOMICS	ss5206473932	Apr 26, 2021 (155)
33	1000G_HIGH_COVERAGE	ss5290924931	Oct 16, 2022 (156)
34	1000G_HIGH_COVERAGE	ss5290924932	Oct 16, 2022 (156)
35	1000G_HIGH_COVERAGE	ss5290924934	Oct 16, 2022 (156)
36	1000G_HIGH_COVERAGE	ss5290924935	Oct 16, 2022 (156)
37	HUGCELL_USP	ss5485662809	Oct 16, 2022 (156)
38	HUGCELL_USP	ss5485662811	Oct 16, 2022 (156)
39	HUGCELL_USP	ss5485662812	Oct 16, 2022 (156)
40	TOMMO_GENOMICS	ss5756312080	Oct 16, 2022 (156)
41	TOMMO_GENOMICS	ss5756312081	Oct 16, 2022 (156)
42	TOMMO_GENOMICS	ss5756312082	Oct 16, 2022 (156)
43	EVA	ss5944581159	Oct 16, 2022 (156)
44	1000Genomes	NC_000012.11 - 56599354	Oct 12, 2018 (152)
45	The Avon Longitudinal Study of Parents and Children	NC_000012.11 - 56599354	Oct 12, 2018 (152)
46	Genetic variation in the Estonian population	NC_000012.11 - 56599354	Oct 12, 2018 (152)
47	The Danish reference pan genome	NC_000012.11 - 56599354	Apr 27, 2020 (154)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 408290234 (NC_000012.12:56205569::G 13590/118636) Row 408290235 (NC_000012.12:56205569::GG 206/118912) Row 408290236 (NC_000012.12:56205569::GGG 25/118922)...	-	Apr 26, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 408290234 (NC_000012.12:56205569::G 13590/118636) Row 408290235 (NC_000012.12:56205569::GG 206/118912) Row 408290236 (NC_000012.12:56205569::GGG 25/118922)...	-	Apr 26, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 408290234 (NC_000012.12:56205569::G 13590/118636) Row 408290235 (NC_000012.12:56205569::GG 206/118912) Row 408290236 (NC_000012.12:56205569::GGG 25/118922)...	-	Apr 26, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 408290234 (NC_000012.12:56205569::G 13590/118636) Row 408290235 (NC_000012.12:56205569::GG 206/118912) Row 408290236 (NC_000012.12:56205569::GGG 25/118922)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 408290234 (NC_000012.12:56205569::G 13590/118636) Row 408290235 (NC_000012.12:56205569::GG 206/118912) Row 408290236 (NC_000012.12:56205569::GGG 25/118922)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 408290234 (NC_000012.12:56205569::G 13590/118636) Row 408290235 (NC_000012.12:56205569::GG 206/118912) Row 408290236 (NC_000012.12:56205569::GGG 25/118922)...	-	Apr 26, 2021 (155)
54	Northern Sweden Submission ignored due to conflicting rows: Row 12334917 (NC_000012.11:56599353::G 70/596) Row 12334918 (NC_000012.11:56599353:G: 1/596)	-	Jul 13, 2019 (153)
55	Northern Sweden Submission ignored due to conflicting rows: Row 12334917 (NC_000012.11:56599353::G 70/596) Row 12334918 (NC_000012.11:56599353:G: 1/596)	-	Jul 13, 2019 (153)
56	8.3KJPN Submission ignored due to conflicting rows: Row 64443237 (NC_000012.11:56599353::G 470/16746) Row 64443238 (NC_000012.11:56599353::GG 42/16746) Row 64443239 (NC_000012.11:56599353:G: 93/16746)	-	Apr 26, 2021 (155)
57	8.3KJPN Submission ignored due to conflicting rows: Row 64443237 (NC_000012.11:56599353::G 470/16746) Row 64443238 (NC_000012.11:56599353::GG 42/16746) Row 64443239 (NC_000012.11:56599353:G: 93/16746)	-	Apr 26, 2021 (155)
58	8.3KJPN Submission ignored due to conflicting rows: Row 64443237 (NC_000012.11:56599353::G 470/16746) Row 64443238 (NC_000012.11:56599353::GG 42/16746) Row 64443239 (NC_000012.11:56599353:G: 93/16746)	-	Apr 26, 2021 (155)
59	14KJPN Submission ignored due to conflicting rows: Row 90149184 (NC_000012.12:56205569::G 795/28254) Row 90149185 (NC_000012.12:56205569:G: 128/28254) Row 90149186 (NC_000012.12:56205569::GG 61/28254)	-	Oct 16, 2022 (156)
60	14KJPN Submission ignored due to conflicting rows: Row 90149184 (NC_000012.12:56205569::G 795/28254) Row 90149185 (NC_000012.12:56205569:G: 128/28254) Row 90149186 (NC_000012.12:56205569::GG 61/28254)	-	Oct 16, 2022 (156)
61	14KJPN Submission ignored due to conflicting rows: Row 90149184 (NC_000012.12:56205569::G 795/28254) Row 90149185 (NC_000012.12:56205569:G: 128/28254) Row 90149186 (NC_000012.12:56205569::GG 61/28254)	-	Oct 16, 2022 (156)
62	UK 10K study - Twins	NC_000012.11 - 56599354	Oct 12, 2018 (152)
63	ALFA	NC_000012.12 - 56205570	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)
rs63527263	May 11, 2012 (137)
rs142811045	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4252372058	NC_000012.12:56205569:GG:	NC_000012.12:56205569:GGGGGGGGGG:G… NC_000012.12:56205569:GGGGGGGGGG:GGGGGGGG	(self)
9009603203	NC_000012.12:56205569:GGGGGGGGGG:G… NC_000012.12:56205569:GGGGGGGGGG:GGGGGGGG	NC_000012.12:56205569:GGGGGGGGGG:G… NC_000012.12:56205569:GGGGGGGGGG:GGGGGGGG	(self)
ss1997053066, ss3739050053, ss3986059999, ss5206473932	NC_000012.11:56599353:G:	NC_000012.12:56205569:GGGGGGGGGG:G… NC_000012.12:56205569:GGGGGGGGGG:GGGGGGGGG	(self)
ss3645254578, ss3693733933, ss4252372057, ss5290924934, ss5485662811, ss5756312081	NC_000012.12:56205569:G:	NC_000012.12:56205569:GGGGGGGGGG:G… NC_000012.12:56205569:GGGGGGGGGG:GGGGGGGGG	(self)
9009603203	NC_000012.12:56205569:GGGGGGGGGG:G… NC_000012.12:56205569:GGGGGGGGGG:GGGGGGGGG	NC_000012.12:56205569:GGGGGGGGGG:G… NC_000012.12:56205569:GGGGGGGGGG:GGGGGGGGG	(self)
ss552218392	NC_000012.10:54885620::G	NC_000012.12:56205569:GGGGGGGGGG:G… NC_000012.12:56205569:GGGGGGGGGG:GGGGGGGGGGG	(self)
ss294753917	NC_000012.10:54885624::G	NC_000012.12:56205569:GGGGGGGGGG:G… NC_000012.12:56205569:GGGGGGGGGG:GGGGGGGGGGG	(self)
57898030, 32146154, 22750283, 355735, 32146154, ss499756472, ss1372202446, ss1574507344, ss1707479222, ss1707479359, ss3677012035, ss3739050052, ss3787235480, ss3792335458, ss3797218225, ss3833139423, ss5206473930, ss5944581159	NC_000012.11:56599353::G	NC_000012.12:56205569:GGGGGGGGGG:G… NC_000012.12:56205569:GGGGGGGGGG:GGGGGGGGGGG	(self)
ss3815848988, ss4252372053, ss5290924931, ss5485662809, ss5756312080	NC_000012.12:56205569::G	NC_000012.12:56205569:GGGGGGGGGG:G… NC_000012.12:56205569:GGGGGGGGGG:GGGGGGGGGGG	(self)
9009603203	NC_000012.12:56205569:GGGGGGGGGG:G… NC_000012.12:56205569:GGGGGGGGGG:GGGGGGGGGGG	NC_000012.12:56205569:GGGGGGGGGG:G… NC_000012.12:56205569:GGGGGGGGGG:GGGGGGGGGGG	(self)
ss3693733932	NC_000012.12:56205570::G	NC_000012.12:56205569:GGGGGGGGGG:G… NC_000012.12:56205569:GGGGGGGGGG:GGGGGGGGGGG	(self)
ss97271803	NT_029419.12:18742659::G	NC_000012.12:56205569:GGGGGGGGGG:G… NC_000012.12:56205569:GGGGGGGGGG:GGGGGGGGGGG	(self)
ss5206473931	NC_000012.11:56599353::GG	NC_000012.12:56205569:GGGGGGGGGG:G… NC_000012.12:56205569:GGGGGGGGGG:GGGGGGGGGGGG	(self)
ss3649844410, ss4252372054, ss5290924932, ss5485662812, ss5756312082	NC_000012.12:56205569::GG	NC_000012.12:56205569:GGGGGGGGGG:G… NC_000012.12:56205569:GGGGGGGGGG:GGGGGGGGGGGG	(self)
9009603203	NC_000012.12:56205569:GGGGGGGGGG:G… NC_000012.12:56205569:GGGGGGGGGG:GGGGGGGGGGGG	NC_000012.12:56205569:GGGGGGGGGG:G… NC_000012.12:56205569:GGGGGGGGGG:GGGGGGGGGGGG	(self)
ss3693733931	NC_000012.12:56205570::GG	NC_000012.12:56205569:GGGGGGGGGG:G… NC_000012.12:56205569:GGGGGGGGGG:GGGGGGGGGGGG	(self)
ss4252372055, ss5290924935	NC_000012.12:56205569::GGG	NC_000012.12:56205569:GGGGGGGGGG:G… NC_000012.12:56205569:GGGGGGGGGG:GGGGGGGGGGGGG	(self)
9009603203	NC_000012.12:56205569:GGGGGGGGGG:G… NC_000012.12:56205569:GGGGGGGGGG:GGGGGGGGGGGGG	NC_000012.12:56205569:GGGGGGGGGG:G… NC_000012.12:56205569:GGGGGGGGGG:GGGGGGGGGGGGG	(self)
ss4252372056	NC_000012.12:56205569::GGGG	NC_000012.12:56205569:GGGGGGGGGG:G… NC_000012.12:56205569:GGGGGGGGGG:GGGGGGGGGGGGGG	(self)
9009603203	NC_000012.12:56205569:GGGGGGGGGG:G… NC_000012.12:56205569:GGGGGGGGGG:GGGGGGGGGGGGGG	NC_000012.12:56205569:GGGGGGGGGG:G… NC_000012.12:56205569:GGGGGGGGGG:GGGGGGGGGGGGGG	(self)
9009603203	NC_000012.12:56205569:GGGGGGGGGG:G… NC_000012.12:56205569:GGGGGGGGGG:GGGGGGGGGGGGGGG	NC_000012.12:56205569:GGGGGGGGGG:G… NC_000012.12:56205569:GGGGGGGGGG:GGGGGGGGGGGGGGG	(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 rs63137960

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.

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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs63137960