Name: rs11376681
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.

rs11376681

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr2:71211603-71211619 (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: delAAA / delAA / delA / dupA / dup…
delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)₄ / dup(A)₈
Variation Type: Indel Insertion and Deletion
Frequency: dupA=0.3093 (1549/5008, 1000G)
delAA=0.0000 (0/1580, ALFA)
delA=0.0000 (0/1580, ALFA) (+ 3 more)
dupA=0.0000 (0/1580, ALFA)
dupAA=0.0000 (0/1580, ALFA)
dupAAA=0.0000 (0/1580, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: PAIP2B : 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	HWEP
Total	Global	1580	AAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
European	Sub	888	AAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
African	Sub	366	AAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
African Others	Sub	10	AAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0	1.0	N/A
African American	Sub	356	AAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
Asian	Sub	74	AAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
East Asian	Sub	54	AAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other Asian	Sub	20	AAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 1	Sub	20	AAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 2	Sub	104	AAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
South Asian	Sub	34	AAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other	Sub	94	AAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00	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").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
1000Genomes	Global	Study-wide	5008	- No frequency provided	dupA=0.3093
1000Genomes	African	Sub	1322	- No frequency provided	dupA=0.3707
1000Genomes	East Asian	Sub	1008	- No frequency provided	dupA=0.0893
1000Genomes	Europe	Sub	1006	- No frequency provided	dupA=0.4503
1000Genomes	South Asian	Sub	978	- No frequency provided	dupA=0.234
1000Genomes	American	Sub	694	- No frequency provided	dupA=0.414
Allele Frequency Aggregator	Total	Global	1580	(A)₁₇=1.0000	delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000
Allele Frequency Aggregator	European	Sub	888	(A)₁₇=1.000	delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000
Allele Frequency Aggregator	African	Sub	366	(A)₁₇=1.000	delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000
Allele Frequency Aggregator	Latin American 2	Sub	104	(A)₁₇=1.000	delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000
Allele Frequency Aggregator	Other	Sub	94	(A)₁₇=1.00	delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00
Allele Frequency Aggregator	Asian	Sub	74	(A)₁₇=1.00	delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00
Allele Frequency Aggregator	South Asian	Sub	34	(A)₁₇=1.00	delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00
Allele Frequency Aggregator	Latin American 1	Sub	20	(A)₁₇=1.00	delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00

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

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 2	NC_000002.12:g.71211617_71211619del
GRCh38.p14 chr 2	NC_000002.12:g.71211618_71211619del
GRCh38.p14 chr 2	NC_000002.12:g.71211619del
GRCh38.p14 chr 2	NC_000002.12:g.71211619dup
GRCh38.p14 chr 2	NC_000002.12:g.71211618_71211619dup
GRCh38.p14 chr 2	NC_000002.12:g.71211617_71211619dup
GRCh38.p14 chr 2	NC_000002.12:g.71211616_71211619dup
GRCh38.p14 chr 2	NC_000002.12:g.71211612_71211619dup
GRCh37.p13 chr 2	NC_000002.11:g.71438747_71438749del
GRCh37.p13 chr 2	NC_000002.11:g.71438748_71438749del
GRCh37.p13 chr 2	NC_000002.11:g.71438749del
GRCh37.p13 chr 2	NC_000002.11:g.71438749dup
GRCh37.p13 chr 2	NC_000002.11:g.71438748_71438749dup
GRCh37.p13 chr 2	NC_000002.11:g.71438747_71438749dup
GRCh37.p13 chr 2	NC_000002.11:g.71438746_71438749dup
GRCh37.p13 chr 2	NC_000002.11:g.71438742_71438749dup

Gene: PAIP2B, poly(A) binding protein interacting protein 2B (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
PAIP2B transcript	NM_020459.1:c.-11-9005_-1… NM_020459.1:c.-11-9005_-11-9003del	N/A	Intron Variant
PAIP2B transcript variant X3	XM_005264310.5:c.-11-9005… XM_005264310.5:c.-11-9005_-11-9003del	N/A	Intron Variant
PAIP2B transcript variant X2	XM_005264311.5:c.-11-9005… XM_005264311.5:c.-11-9005_-11-9003del	N/A	Intron Variant
PAIP2B transcript variant X1	XM_011532842.4:c.53-9005_… XM_011532842.4:c.53-9005_53-9003del	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	(A)₁₇=	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄	dup(A)₈
GRCh38.p14 chr 2	NC_000002.12:g.71211603_71211619=	NC_000002.12:g.71211617_71211619del	NC_000002.12:g.71211618_71211619del	NC_000002.12:g.71211619del	NC_000002.12:g.71211619dup	NC_000002.12:g.71211618_71211619dup	NC_000002.12:g.71211617_71211619dup	NC_000002.12:g.71211616_71211619dup	NC_000002.12:g.71211612_71211619dup
GRCh37.p13 chr 2	NC_000002.11:g.71438733_71438749=	NC_000002.11:g.71438747_71438749del	NC_000002.11:g.71438748_71438749del	NC_000002.11:g.71438749del	NC_000002.11:g.71438749dup	NC_000002.11:g.71438748_71438749dup	NC_000002.11:g.71438747_71438749dup	NC_000002.11:g.71438746_71438749dup	NC_000002.11:g.71438742_71438749dup
PAIP2B transcript	NM_020459.1:c.-11-9003=	NM_020459.1:c.-11-9005_-11-9003del	NM_020459.1:c.-11-9004_-11-9003del	NM_020459.1:c.-11-9003del	NM_020459.1:c.-11-9003dup	NM_020459.1:c.-11-9004_-11-9003dup	NM_020459.1:c.-11-9005_-11-9003dup	NM_020459.1:c.-11-9006_-11-9003dup	NM_020459.1:c.-11-9010_-11-9003dup
PAIP2B transcript variant X1	XM_005264310.1:c.-11-9003=	XM_005264310.1:c.-11-9005_-11-9003del	XM_005264310.1:c.-11-9004_-11-9003del	XM_005264310.1:c.-11-9003del	XM_005264310.1:c.-11-9003dup	XM_005264310.1:c.-11-9004_-11-9003dup	XM_005264310.1:c.-11-9005_-11-9003dup	XM_005264310.1:c.-11-9006_-11-9003dup	XM_005264310.1:c.-11-9010_-11-9003dup
PAIP2B transcript variant X3	XM_005264310.5:c.-11-9003=	XM_005264310.5:c.-11-9005_-11-9003del	XM_005264310.5:c.-11-9004_-11-9003del	XM_005264310.5:c.-11-9003del	XM_005264310.5:c.-11-9003dup	XM_005264310.5:c.-11-9004_-11-9003dup	XM_005264310.5:c.-11-9005_-11-9003dup	XM_005264310.5:c.-11-9006_-11-9003dup	XM_005264310.5:c.-11-9010_-11-9003dup
PAIP2B transcript variant X2	XM_005264311.1:c.-11-9003=	XM_005264311.1:c.-11-9005_-11-9003del	XM_005264311.1:c.-11-9004_-11-9003del	XM_005264311.1:c.-11-9003del	XM_005264311.1:c.-11-9003dup	XM_005264311.1:c.-11-9004_-11-9003dup	XM_005264311.1:c.-11-9005_-11-9003dup	XM_005264311.1:c.-11-9006_-11-9003dup	XM_005264311.1:c.-11-9010_-11-9003dup
PAIP2B transcript variant X2	XM_005264311.5:c.-11-9003=	XM_005264311.5:c.-11-9005_-11-9003del	XM_005264311.5:c.-11-9004_-11-9003del	XM_005264311.5:c.-11-9003del	XM_005264311.5:c.-11-9003dup	XM_005264311.5:c.-11-9004_-11-9003dup	XM_005264311.5:c.-11-9005_-11-9003dup	XM_005264311.5:c.-11-9006_-11-9003dup	XM_005264311.5:c.-11-9010_-11-9003dup
PAIP2B transcript variant X1	XM_011532842.4:c.53-9003=	XM_011532842.4:c.53-9005_53-9003del	XM_011532842.4:c.53-9004_53-9003del	XM_011532842.4:c.53-9003del	XM_011532842.4:c.53-9003dup	XM_011532842.4:c.53-9004_53-9003dup	XM_011532842.4:c.53-9005_53-9003dup	XM_011532842.4:c.53-9006_53-9003dup	XM_011532842.4:c.53-9010_53-9003dup

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#.

47 SubSNP, 16 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss41692770	Dec 03, 2013 (138)
2	HUMANGENOME_JCVI	ss95276290	Feb 13, 2009 (137)
3	HUMANGENOME_JCVI	ss96725063	Mar 15, 2016 (147)
4	GMI	ss287700099	May 09, 2011 (136)
5	PJP	ss294989343	May 09, 2011 (136)
6	BILGI_BIOE	ss666152539	Jan 10, 2018 (151)
7	1000GENOMES	ss1368316677	Aug 21, 2014 (142)
8	SWEGEN	ss2989720856	Jan 10, 2018 (151)
9	MCHAISSO	ss3064792386	Nov 08, 2017 (151)
10	MCHAISSO	ss3065747219	Nov 08, 2017 (151)
11	URBANLAB	ss3647061687	Oct 11, 2018 (152)
12	EVA_DECODE	ss3704155584	Jul 13, 2019 (153)
13	EVA_DECODE	ss3704155585	Jul 13, 2019 (153)
14	EVA_DECODE	ss3704155586	Jul 13, 2019 (153)
15	EVA_DECODE	ss3704155587	Jul 13, 2019 (153)
16	EVA_DECODE	ss3704155588	Jul 13, 2019 (153)
17	PACBIO	ss3783896346	Jul 13, 2019 (153)
18	PACBIO	ss3789477588	Jul 13, 2019 (153)
19	PACBIO	ss3794350542	Jul 13, 2019 (153)
20	KHV_HUMAN_GENOMES	ss3801292546	Jul 13, 2019 (153)
21	EVA	ss3827047396	Apr 25, 2020 (154)
22	EVA	ss3836932884	Apr 25, 2020 (154)
23	EVA	ss3842348952	Apr 25, 2020 (154)
24	KOGIC	ss3948016356	Apr 25, 2020 (154)
25	KOGIC	ss3948016357	Apr 25, 2020 (154)
26	GNOMAD	ss4043692767	Apr 26, 2021 (155)
27	GNOMAD	ss4043692768	Apr 26, 2021 (155)
28	GNOMAD	ss4043692769	Apr 26, 2021 (155)
29	GNOMAD	ss4043692770	Apr 26, 2021 (155)
30	GNOMAD	ss4043692772	Apr 26, 2021 (155)
31	GNOMAD	ss4043692773	Apr 26, 2021 (155)
32	GNOMAD	ss4043692774	Apr 26, 2021 (155)
33	TOMMO_GENOMICS	ss5151973643	Apr 26, 2021 (155)
34	TOMMO_GENOMICS	ss5151973644	Apr 26, 2021 (155)
35	1000G_HIGH_COVERAGE	ss5248527757	Oct 12, 2022 (156)
36	1000G_HIGH_COVERAGE	ss5248527758	Oct 12, 2022 (156)
37	1000G_HIGH_COVERAGE	ss5248527759	Oct 12, 2022 (156)
38	1000G_HIGH_COVERAGE	ss5248527760	Oct 12, 2022 (156)
39	HUGCELL_USP	ss5448687123	Oct 12, 2022 (156)
40	HUGCELL_USP	ss5448687124	Oct 12, 2022 (156)
41	HUGCELL_USP	ss5448687125	Oct 12, 2022 (156)
42	HUGCELL_USP	ss5448687126	Oct 12, 2022 (156)
43	TOMMO_GENOMICS	ss5680772784	Oct 12, 2022 (156)
44	TOMMO_GENOMICS	ss5680772785	Oct 12, 2022 (156)
45	TOMMO_GENOMICS	ss5680772787	Oct 12, 2022 (156)
46	EVA	ss5820278635	Oct 12, 2022 (156)
47	EVA	ss5820278636	Oct 12, 2022 (156)
48	1000Genomes	NC_000002.11 - 71438733	Oct 11, 2018 (152)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 62104914 (NC_000002.12:71211602::A 66002/123478) Row 62104915 (NC_000002.12:71211602::AA 360/123564) Row 62104916 (NC_000002.12:71211602::AAA 3/123602)...	-	Apr 26, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 62104914 (NC_000002.12:71211602::A 66002/123478) Row 62104915 (NC_000002.12:71211602::AA 360/123564) Row 62104916 (NC_000002.12:71211602::AAA 3/123602)...	-	Apr 26, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 62104914 (NC_000002.12:71211602::A 66002/123478) Row 62104915 (NC_000002.12:71211602::AA 360/123564) Row 62104916 (NC_000002.12:71211602::AAA 3/123602)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 62104914 (NC_000002.12:71211602::A 66002/123478) Row 62104915 (NC_000002.12:71211602::AA 360/123564) Row 62104916 (NC_000002.12:71211602::AAA 3/123602)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 62104914 (NC_000002.12:71211602::A 66002/123478) Row 62104915 (NC_000002.12:71211602::AA 360/123564) Row 62104916 (NC_000002.12:71211602::AAA 3/123602)...	-	Apr 26, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 62104914 (NC_000002.12:71211602::A 66002/123478) Row 62104915 (NC_000002.12:71211602::AA 360/123564) Row 62104916 (NC_000002.12:71211602::AAA 3/123602)...	-	Apr 26, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 62104914 (NC_000002.12:71211602::A 66002/123478) Row 62104915 (NC_000002.12:71211602::AA 360/123564) Row 62104916 (NC_000002.12:71211602::AAA 3/123602)...	-	Apr 26, 2021 (155)
56	Korean Genome Project Submission ignored due to conflicting rows: Row 4394357 (NC_000002.12:71211602:A: 239/1832) Row 4394358 (NC_000002.12:71211603::A 376/1832)	-	Apr 25, 2020 (154)
57	Korean Genome Project Submission ignored due to conflicting rows: Row 4394357 (NC_000002.12:71211602:A: 239/1832) Row 4394358 (NC_000002.12:71211603::A 376/1832)	-	Apr 25, 2020 (154)
58	8.3KJPN Submission ignored due to conflicting rows: Row 9942950 (NC_000002.11:71438732::A 2098/16760) Row 9942951 (NC_000002.11:71438732:A: 92/16760)	-	Apr 26, 2021 (155)
59	8.3KJPN Submission ignored due to conflicting rows: Row 9942950 (NC_000002.11:71438732::A 2098/16760) Row 9942951 (NC_000002.11:71438732:A: 92/16760)	-	Apr 26, 2021 (155)
60	14KJPN Submission ignored due to conflicting rows: Row 14609888 (NC_000002.12:71211602::A 3528/28258) Row 14609889 (NC_000002.12:71211602:A: 155/28258) Row 14609891 (NC_000002.12:71211602::AA 1/28258)	-	Oct 12, 2022 (156)
61	14KJPN Submission ignored due to conflicting rows: Row 14609888 (NC_000002.12:71211602::A 3528/28258) Row 14609889 (NC_000002.12:71211602:A: 155/28258) Row 14609891 (NC_000002.12:71211602::AA 1/28258)	-	Oct 12, 2022 (156)
62	14KJPN Submission ignored due to conflicting rows: Row 14609888 (NC_000002.12:71211602::A 3528/28258) Row 14609889 (NC_000002.12:71211602:A: 155/28258) Row 14609891 (NC_000002.12:71211602::AA 1/28258)	-	Oct 12, 2022 (156)
63	ALFA	NC_000002.12 - 71211603	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)
rs149238022	Oct 17, 2011 (136)
rs376113728	May 13, 2013 (138)
rs11430312	May 11, 2012 (137)
rs36115949	May 11, 2012 (137)
rs70959218	May 11, 2012 (137)
rs71678086	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4043692774	NC_000002.12:71211602:AAA:	NC_000002.12:71211602:AAAAAAAAAAAA… NC_000002.12:71211602:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3704155588, ss4043692773, ss5248527760, ss5448687125	NC_000002.12:71211602:AA:	NC_000002.12:71211602:AAAAAAAAAAAA… NC_000002.12:71211602:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
11665371011	NC_000002.12:71211602:AAAAAAAAAAAA… NC_000002.12:71211602:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000002.12:71211602:AAAAAAAAAAAA… NC_000002.12:71211602:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss666152539, ss2989720856, ss5151973644	NC_000002.11:71438732:A:	NC_000002.12:71211602:AAAAAAAAAAAA… NC_000002.12:71211602:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3948016356, ss4043692772, ss5248527757, ss5448687123, ss5680772785	NC_000002.12:71211602:A:	NC_000002.12:71211602:AAAAAAAAAAAA… NC_000002.12:71211602:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
11665371011	NC_000002.12:71211602:AAAAAAAAAAAA… NC_000002.12:71211602:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000002.12:71211602:AAAAAAAAAAAA… NC_000002.12:71211602:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3704155587	NC_000002.12:71211603:A:	NC_000002.12:71211602:AAAAAAAAAAAA… NC_000002.12:71211602:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss96725063, ss287700099	NT_022184.15:50260619:A:	NC_000002.12:71211602:AAAAAAAAAAAA… NC_000002.12:71211602:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss41692770	NT_022184.15:50260635:A:	NC_000002.12:71211602:AAAAAAAAAAAA… NC_000002.12:71211602:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss294989343	NC_000002.10:71292241::A	NC_000002.12:71211602:AAAAAAAAAAAA… NC_000002.12:71211602:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
8746760, ss1368316677, ss3783896346, ss3789477588, ss3794350542, ss3827047396, ss3836932884, ss5151973643, ss5820278635	NC_000002.11:71438732::A	NC_000002.12:71211602:AAAAAAAAAAAA… NC_000002.12:71211602:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3064792386, ss3065747219, ss3647061687, ss3801292546, ss3842348952, ss4043692767, ss5248527758, ss5448687124, ss5680772784	NC_000002.12:71211602::A	NC_000002.12:71211602:AAAAAAAAAAAA… NC_000002.12:71211602:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
11665371011	NC_000002.12:71211602:AAAAAAAAAAAA… NC_000002.12:71211602:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000002.12:71211602:AAAAAAAAAAAA… NC_000002.12:71211602:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3948016357	NC_000002.12:71211603::A	NC_000002.12:71211602:AAAAAAAAAAAA… NC_000002.12:71211602:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3704155586	NC_000002.12:71211604::A	NC_000002.12:71211602:AAAAAAAAAAAA… NC_000002.12:71211602:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss96725063	NT_022184.15:50260619:A:AA	NC_000002.12:71211602:AAAAAAAAAAAA… NC_000002.12:71211602:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss95276290	NT_022184.15:50260636::A	NC_000002.12:71211602:AAAAAAAAAAAA… NC_000002.12:71211602:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss5820278636	NC_000002.11:71438732::AA	NC_000002.12:71211602:AAAAAAAAAAAA… NC_000002.12:71211602:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA
ss4043692768, ss5248527759, ss5448687126, ss5680772787	NC_000002.12:71211602::AA	NC_000002.12:71211602:AAAAAAAAAAAA… NC_000002.12:71211602:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
11665371011	NC_000002.12:71211602:AAAAAAAAAAAA… NC_000002.12:71211602:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000002.12:71211602:AAAAAAAAAAAA… NC_000002.12:71211602:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss3704155585	NC_000002.12:71211604::AA	NC_000002.12:71211602:AAAAAAAAAAAA… NC_000002.12:71211602:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss4043692769	NC_000002.12:71211602::AAA	NC_000002.12:71211602:AAAAAAAAAAAA… NC_000002.12:71211602:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
11665371011	NC_000002.12:71211602:AAAAAAAAAAAA… NC_000002.12:71211602:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000002.12:71211602:AAAAAAAAAAAA… NC_000002.12:71211602:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss4043692770	NC_000002.12:71211602::AAAA	NC_000002.12:71211602:AAAAAAAAAAAA… NC_000002.12:71211602:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss3704155584	NC_000002.12:71211604::AAAAAAAA	NC_000002.12:71211602:AAAAAAAAAAAA… NC_000002.12:71211602:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(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 rs11376681

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

rs11376681