Name: rs11343831
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.

rs11343831

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr2:74910290-74910304 (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)₅ / del(T)₄ / delTTT / delTT…
del(T)₅ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / ins(T)₁₆
Variation Type: Indel Insertion and Deletion
Frequency: delTTT=0.1219 (1032/8466, ALFA)
delTTT=0.2242 (1123/5008, 1000G)
delTTT=0.2439 (940/3854, ALSPAC)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: LINC01291 : 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	8466	TTTTTTTTTTTTTTT=0.7842	TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.1219, TTTTTTTTTTTTTT=0.0893, TTTTTTTTTTTTTTTT=0.0045, TTTTTTTTTTTTT=0.0001, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000	0.782201	0.032698	0.185101	32
European	Sub	7438	TTTTTTTTTTTTTTT=0.7546	TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.1386, TTTTTTTTTTTTTT=0.1015, TTTTTTTTTTTTTTTT=0.0051, TTTTTTTTTTTTT=0.0001, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000	0.74534	0.038282	0.216378	29
African	Sub	654	TTTTTTTTTTTTTTT=1.000	TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	16	TTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	638	TTTTTTTTTTTTTTT=1.000	TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	26	TTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	18	TTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	8	TTTTTTTTTTTTTTT=1.0	TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	46	TTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	118	TTTTTTTTTTTTTTT=1.000	TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	34	TTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	150	TTTTTTTTTTTTTTT=0.987	TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.007, TTTTTTTTTTTTTT=0.007, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000	0.986486	0.0	0.013514	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	8466	(T)₁₅=0.7842	del(T)₄=0.0000, delTTT=0.1219, delTT=0.0001, delT=0.0893, dupT=0.0045, dupTT=0.0000, dupTTT=0.0000
Allele Frequency Aggregator	European	Sub	7438	(T)₁₅=0.7546	del(T)₄=0.0000, delTTT=0.1386, delTT=0.0001, delT=0.1015, dupT=0.0051, dupTT=0.0000, dupTTT=0.0000
Allele Frequency Aggregator	African	Sub	654	(T)₁₅=1.000	del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000
Allele Frequency Aggregator	Other	Sub	150	(T)₁₅=0.987	del(T)₄=0.000, delTTT=0.007, delTT=0.000, delT=0.007, dupT=0.000, dupTT=0.000, dupTTT=0.000
Allele Frequency Aggregator	Latin American 2	Sub	118	(T)₁₅=1.000	del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000
Allele Frequency Aggregator	Latin American 1	Sub	46	(T)₁₅=1.00	del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00
Allele Frequency Aggregator	South Asian	Sub	34	(T)₁₅=1.00	del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00
Allele Frequency Aggregator	Asian	Sub	26	(T)₁₅=1.00	del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00
1000Genomes	Global	Study-wide	5008	(T)₁₅=0.7758	delTTT=0.2242
1000Genomes	African	Sub	1322	(T)₁₅=0.9266	delTTT=0.0734
1000Genomes	East Asian	Sub	1008	(T)₁₅=0.7004	delTTT=0.2996
1000Genomes	Europe	Sub	1006	(T)₁₅=0.7863	delTTT=0.2137
1000Genomes	South Asian	Sub	978	(T)₁₅=0.730	delTTT=0.270
1000Genomes	American	Sub	694	(T)₁₅=0.647	delTTT=0.353
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	(T)₁₅=0.7561	delTTT=0.2439

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.74910300_74910304del
GRCh38.p14 chr 2	NC_000002.12:g.74910301_74910304del
GRCh38.p14 chr 2	NC_000002.12:g.74910302_74910304del
GRCh38.p14 chr 2	NC_000002.12:g.74910303_74910304del
GRCh38.p14 chr 2	NC_000002.12:g.74910304del
GRCh38.p14 chr 2	NC_000002.12:g.74910304dup
GRCh38.p14 chr 2	NC_000002.12:g.74910303_74910304dup
GRCh38.p14 chr 2	NC_000002.12:g.74910302_74910304dup
GRCh38.p14 chr 2	NC_000002.12:g.74910304_74910305insTTTTTTTTTTTTTTTT
GRCh37.p13 chr 2	NC_000002.11:g.75137427_75137431del
GRCh37.p13 chr 2	NC_000002.11:g.75137428_75137431del
GRCh37.p13 chr 2	NC_000002.11:g.75137429_75137431del
GRCh37.p13 chr 2	NC_000002.11:g.75137430_75137431del
GRCh37.p13 chr 2	NC_000002.11:g.75137431del
GRCh37.p13 chr 2	NC_000002.11:g.75137431dup
GRCh37.p13 chr 2	NC_000002.11:g.75137430_75137431dup
GRCh37.p13 chr 2	NC_000002.11:g.75137429_75137431dup
GRCh37.p13 chr 2	NC_000002.11:g.75137431_75137432insTTTTTTTTTTTTTTTT

Gene: LINC01291, long intergenic non-protein coding RNA 1291 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LINC01291 transcript	NR_125792.1: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	(T)₁₅=	del(T)₅	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	ins(T)₁₆
GRCh38.p14 chr 2	NC_000002.12:g.74910290_74910304=	NC_000002.12:g.74910300_74910304del	NC_000002.12:g.74910301_74910304del	NC_000002.12:g.74910302_74910304del	NC_000002.12:g.74910303_74910304del	NC_000002.12:g.74910304del	NC_000002.12:g.74910304dup	NC_000002.12:g.74910303_74910304dup	NC_000002.12:g.74910302_74910304dup	NC_000002.12:g.74910304_74910305insTTTTTTTTTTTTTTTT
GRCh37.p13 chr 2	NC_000002.11:g.75137417_75137431=	NC_000002.11:g.75137427_75137431del	NC_000002.11:g.75137428_75137431del	NC_000002.11:g.75137429_75137431del	NC_000002.11:g.75137430_75137431del	NC_000002.11:g.75137431del	NC_000002.11:g.75137431dup	NC_000002.11:g.75137430_75137431dup	NC_000002.11:g.75137429_75137431dup	NC_000002.11:g.75137431_75137432insTTTTTTTTTTTTTTTT

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, 29 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss41817331	Dec 03, 2013 (138)
2	HGSV	ss80183753	Oct 11, 2018 (152)
3	BCMHGSC_JDW	ss103628334	Dec 06, 2013 (138)
4	GMI	ss288180313	May 04, 2012 (137)
5	GMI	ss288180315	May 04, 2012 (137)
6	SSMP	ss663326277	Apr 01, 2015 (144)
7	BILGI_BIOE	ss666153169	Apr 25, 2013 (138)
8	1000GENOMES	ss1368345931	Aug 21, 2014 (142)
9	DDI	ss1536294035	Apr 01, 2015 (144)
10	EVA_UK10K_TWINSUK	ss1702744869	Apr 01, 2015 (144)
11	EVA_UK10K_ALSPAC	ss1702744871	Apr 01, 2015 (144)
12	EVA_UK10K_TWINSUK	ss1710009839	Apr 01, 2015 (144)
13	EVA_UK10K_ALSPAC	ss1710009840	Apr 01, 2015 (144)
14	SWEGEN	ss2989759898	Nov 08, 2017 (151)
15	BEROUKHIMLAB	ss3644094625	Oct 11, 2018 (152)
16	EVA_DECODE	ss3704203702	Jul 13, 2019 (153)
17	EVA_DECODE	ss3704203703	Jul 13, 2019 (153)
18	EVA_DECODE	ss3704203704	Jul 13, 2019 (153)
19	EVA_DECODE	ss3704203705	Jul 13, 2019 (153)
20	EVA_DECODE	ss3704203706	Jul 13, 2019 (153)
21	ACPOP	ss3728566498	Jul 13, 2019 (153)
22	ACPOP	ss3728566499	Jul 13, 2019 (153)
23	ACPOP	ss3728566500	Jul 13, 2019 (153)
24	PACBIO	ss3783901230	Jul 13, 2019 (153)
25	PACBIO	ss3789481197	Jul 13, 2019 (153)
26	PACBIO	ss3794354170	Jul 13, 2019 (153)
27	KHV_HUMAN_GENOMES	ss3801319646	Jul 13, 2019 (153)
28	KHV_HUMAN_GENOMES	ss3801319647	Jul 13, 2019 (153)
29	EVA	ss3827057821	Apr 25, 2020 (154)
30	EVA	ss3836937826	Apr 25, 2020 (154)
31	EVA	ss3842354003	Apr 25, 2020 (154)
32	KOGIC	ss3948068321	Apr 25, 2020 (154)
33	KOGIC	ss3948068322	Apr 25, 2020 (154)
34	KOGIC	ss3948068323	Apr 25, 2020 (154)
35	KOGIC	ss3948068324	Apr 25, 2020 (154)
36	GNOMAD	ss4044144265	Apr 26, 2021 (155)
37	GNOMAD	ss4044144266	Apr 26, 2021 (155)
38	GNOMAD	ss4044144267	Apr 26, 2021 (155)
39	GNOMAD	ss4044144269	Apr 26, 2021 (155)
40	GNOMAD	ss4044144270	Apr 26, 2021 (155)
41	GNOMAD	ss4044144271	Apr 26, 2021 (155)
42	GNOMAD	ss4044144272	Apr 26, 2021 (155)
43	GNOMAD	ss4044144273	Apr 26, 2021 (155)
44	TOMMO_GENOMICS	ss5152088295	Apr 26, 2021 (155)
45	TOMMO_GENOMICS	ss5152088296	Apr 26, 2021 (155)
46	TOMMO_GENOMICS	ss5152088297	Apr 26, 2021 (155)
47	TOMMO_GENOMICS	ss5152088298	Apr 26, 2021 (155)
48	1000G_HIGH_COVERAGE	ss5248615322	Oct 12, 2022 (156)
49	1000G_HIGH_COVERAGE	ss5248615323	Oct 12, 2022 (156)
50	1000G_HIGH_COVERAGE	ss5248615324	Oct 12, 2022 (156)
51	1000G_HIGH_COVERAGE	ss5248615325	Oct 12, 2022 (156)
52	1000G_HIGH_COVERAGE	ss5248615326	Oct 12, 2022 (156)
53	1000G_HIGH_COVERAGE	ss5248615327	Oct 12, 2022 (156)
54	HUGCELL_USP	ss5448765545	Oct 12, 2022 (156)
55	HUGCELL_USP	ss5448765546	Oct 12, 2022 (156)
56	HUGCELL_USP	ss5448765547	Oct 12, 2022 (156)
57	TOMMO_GENOMICS	ss5680923652	Oct 12, 2022 (156)
58	TOMMO_GENOMICS	ss5680923653	Oct 12, 2022 (156)
59	TOMMO_GENOMICS	ss5680923654	Oct 12, 2022 (156)
60	TOMMO_GENOMICS	ss5680923655	Oct 12, 2022 (156)
61	TOMMO_GENOMICS	ss5680923656	Oct 12, 2022 (156)
62	EVA	ss5820310314	Oct 12, 2022 (156)
63	EVA	ss5820310315	Oct 12, 2022 (156)
64	EVA	ss5820310316	Oct 12, 2022 (156)
65	EVA	ss5931008604	Oct 12, 2022 (156)
66	1000Genomes	NC_000002.11 - 75137417	Oct 11, 2018 (152)
67	The Avon Longitudinal Study of Parents and Children	NC_000002.11 - 75137417	Oct 11, 2018 (152)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 62860271 (NC_000002.12:74910289::T 14882/132638) Row 62860272 (NC_000002.12:74910289::TT 50/132728) Row 62860273 (NC_000002.12:74910289::TTTTTTTTTTTTTTTT 1/132732)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 62860271 (NC_000002.12:74910289::T 14882/132638) Row 62860272 (NC_000002.12:74910289::TT 50/132728) Row 62860273 (NC_000002.12:74910289::TTTTTTTTTTTTTTTT 1/132732)...	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 62860271 (NC_000002.12:74910289::T 14882/132638) Row 62860272 (NC_000002.12:74910289::TT 50/132728) Row 62860273 (NC_000002.12:74910289::TTTTTTTTTTTTTTTT 1/132732)...	-	Apr 26, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 62860271 (NC_000002.12:74910289::T 14882/132638) Row 62860272 (NC_000002.12:74910289::TT 50/132728) Row 62860273 (NC_000002.12:74910289::TTTTTTTTTTTTTTTT 1/132732)...	-	Apr 26, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 62860271 (NC_000002.12:74910289::T 14882/132638) Row 62860272 (NC_000002.12:74910289::TT 50/132728) Row 62860273 (NC_000002.12:74910289::TTTTTTTTTTTTTTTT 1/132732)...	-	Apr 26, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 62860271 (NC_000002.12:74910289::T 14882/132638) Row 62860272 (NC_000002.12:74910289::TT 50/132728) Row 62860273 (NC_000002.12:74910289::TTTTTTTTTTTTTTTT 1/132732)...	-	Apr 26, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 62860271 (NC_000002.12:74910289::T 14882/132638) Row 62860272 (NC_000002.12:74910289::TT 50/132728) Row 62860273 (NC_000002.12:74910289::TTTTTTTTTTTTTTTT 1/132732)...	-	Apr 26, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 62860271 (NC_000002.12:74910289::T 14882/132638) Row 62860272 (NC_000002.12:74910289::TT 50/132728) Row 62860273 (NC_000002.12:74910289::TTTTTTTTTTTTTTTT 1/132732)...	-	Apr 26, 2021 (155)
76	Korean Genome Project Submission ignored due to conflicting rows: Row 4446322 (NC_000002.12:74910289:TTT: 529/1832) Row 4446323 (NC_000002.12:74910291:T: 399/1832) Row 4446324 (NC_000002.12:74910290:TT: 17/1832)...	-	Apr 25, 2020 (154)
77	Korean Genome Project Submission ignored due to conflicting rows: Row 4446322 (NC_000002.12:74910289:TTT: 529/1832) Row 4446323 (NC_000002.12:74910291:T: 399/1832) Row 4446324 (NC_000002.12:74910290:TT: 17/1832)...	-	Apr 25, 2020 (154)
78	Korean Genome Project Submission ignored due to conflicting rows: Row 4446322 (NC_000002.12:74910289:TTT: 529/1832) Row 4446323 (NC_000002.12:74910291:T: 399/1832) Row 4446324 (NC_000002.12:74910290:TT: 17/1832)...	-	Apr 25, 2020 (154)
79	Korean Genome Project Submission ignored due to conflicting rows: Row 4446322 (NC_000002.12:74910289:TTT: 529/1832) Row 4446323 (NC_000002.12:74910291:T: 399/1832) Row 4446324 (NC_000002.12:74910290:TT: 17/1832)...	-	Apr 25, 2020 (154)
80	Northern Sweden Submission ignored due to conflicting rows: Row 1851363 (NC_000002.11:75137416:TTT: 128/600) Row 1851364 (NC_000002.11:75137416:T: 127/600) Row 1851365 (NC_000002.11:75137416::T 4/600)	-	Jul 13, 2019 (153)
81	Northern Sweden Submission ignored due to conflicting rows: Row 1851363 (NC_000002.11:75137416:TTT: 128/600) Row 1851364 (NC_000002.11:75137416:T: 127/600) Row 1851365 (NC_000002.11:75137416::T 4/600)	-	Jul 13, 2019 (153)
82	Northern Sweden Submission ignored due to conflicting rows: Row 1851363 (NC_000002.11:75137416:TTT: 128/600) Row 1851364 (NC_000002.11:75137416:T: 127/600) Row 1851365 (NC_000002.11:75137416::T 4/600)	-	Jul 13, 2019 (153)
83	8.3KJPN Submission ignored due to conflicting rows: Row 10057602 (NC_000002.11:75137416:TTT: 5118/16756) Row 10057603 (NC_000002.11:75137416:T: 2350/16756) Row 10057604 (NC_000002.11:75137416:TT: 42/16756)...	-	Apr 26, 2021 (155)
84	8.3KJPN Submission ignored due to conflicting rows: Row 10057602 (NC_000002.11:75137416:TTT: 5118/16756) Row 10057603 (NC_000002.11:75137416:T: 2350/16756) Row 10057604 (NC_000002.11:75137416:TT: 42/16756)...	-	Apr 26, 2021 (155)
85	8.3KJPN Submission ignored due to conflicting rows: Row 10057602 (NC_000002.11:75137416:TTT: 5118/16756) Row 10057603 (NC_000002.11:75137416:T: 2350/16756) Row 10057604 (NC_000002.11:75137416:TT: 42/16756)...	-	Apr 26, 2021 (155)
86	8.3KJPN Submission ignored due to conflicting rows: Row 10057602 (NC_000002.11:75137416:TTT: 5118/16756) Row 10057603 (NC_000002.11:75137416:T: 2350/16756) Row 10057604 (NC_000002.11:75137416:TT: 42/16756)...	-	Apr 26, 2021 (155)
87	14KJPN Submission ignored due to conflicting rows: Row 14760756 (NC_000002.12:74910289:T: 4006/28258) Row 14760757 (NC_000002.12:74910289::T 30/28258) Row 14760758 (NC_000002.12:74910289:TTT: 8603/28258)...	-	Oct 12, 2022 (156)
88	14KJPN Submission ignored due to conflicting rows: Row 14760756 (NC_000002.12:74910289:T: 4006/28258) Row 14760757 (NC_000002.12:74910289::T 30/28258) Row 14760758 (NC_000002.12:74910289:TTT: 8603/28258)...	-	Oct 12, 2022 (156)
89	14KJPN Submission ignored due to conflicting rows: Row 14760756 (NC_000002.12:74910289:T: 4006/28258) Row 14760757 (NC_000002.12:74910289::T 30/28258) Row 14760758 (NC_000002.12:74910289:TTT: 8603/28258)...	-	Oct 12, 2022 (156)
90	14KJPN Submission ignored due to conflicting rows: Row 14760756 (NC_000002.12:74910289:T: 4006/28258) Row 14760757 (NC_000002.12:74910289::T 30/28258) Row 14760758 (NC_000002.12:74910289:TTT: 8603/28258)...	-	Oct 12, 2022 (156)
91	14KJPN Submission ignored due to conflicting rows: Row 14760756 (NC_000002.12:74910289:T: 4006/28258) Row 14760757 (NC_000002.12:74910289::T 30/28258) Row 14760758 (NC_000002.12:74910289:TTT: 8603/28258)...	-	Oct 12, 2022 (156)
92	UK 10K study - Twins Submission ignored due to conflicting rows: Row 4924204 (NC_000002.11:75137418:T: 431/3708) Row 4924205 (NC_000002.11:75137416:TTT: 870/3708)	-	Apr 25, 2020 (154)
93	UK 10K study - Twins	-	Oct 11, 2018 (152)
94	ALFA	NC_000002.12 - 74910290	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)
rs35925186	May 11, 2012 (137)
rs201365538	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4044144273	NC_000002.12:74910289:TTTTT:	NC_000002.12:74910289:TTTTTTTTTTTT… NC_000002.12:74910289:TTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
ss5820310315	NC_000002.11:75137416:TTTT:	NC_000002.12:74910289:TTTTTTTTTTTT… NC_000002.12:74910289:TTTTTTTTTTTTTTT:TTTTTTTTTTT
ss3704203702, ss4044144272, ss5248615325, ss5680923655	NC_000002.12:74910289:TTTT:	NC_000002.12:74910289:TTTTTTTTTTTT… NC_000002.12:74910289:TTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
3613201407	NC_000002.12:74910289:TTTTTTTTTTTT… NC_000002.12:74910289:TTTTTTTTTTTTTTT:TTTTTTTTTTT	NC_000002.12:74910289:TTTTTTTTTTTT… NC_000002.12:74910289:TTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss288180315	NC_000002.10:74990924:TTT:	NC_000002.12:74910289:TTTTTTTTTTTT… NC_000002.12:74910289:TTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
8850452, 4924205, ss663326277, ss666153169, ss1368345931, ss1536294035, ss1702744869, ss1702744871, ss2989759898, ss3644094625, ss3728566498, ss3783901230, ss3789481197, ss3794354170, ss5152088295, ss5820310314	NC_000002.11:75137416:TTT:	NC_000002.12:74910289:TTTTTTTTTTTT… NC_000002.12:74910289:TTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss3801319647, ss3948068321, ss4044144271, ss5248615322, ss5448765545, ss5680923654, ss5931008604	NC_000002.12:74910289:TTT:	NC_000002.12:74910289:TTTTTTTTTTTT… NC_000002.12:74910289:TTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
3613201407	NC_000002.12:74910289:TTTTTTTTTTTT… NC_000002.12:74910289:TTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000002.12:74910289:TTTTTTTTTTTT… NC_000002.12:74910289:TTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss3704203703	NC_000002.12:74910290:TTT:	NC_000002.12:74910289:TTTTTTTTTTTT… NC_000002.12:74910289:TTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss5152088297	NC_000002.11:75137416:TT:	NC_000002.12:74910289:TTTTTTTTTTTT… NC_000002.12:74910289:TTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4044144270, ss5248615326, ss5680923656	NC_000002.12:74910289:TT:	NC_000002.12:74910289:TTTTTTTTTTTT… NC_000002.12:74910289:TTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
3613201407	NC_000002.12:74910289:TTTTTTTTTTTT… NC_000002.12:74910289:TTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000002.12:74910289:TTTTTTTTTTTT… NC_000002.12:74910289:TTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss3948068323	NC_000002.12:74910290:TT:	NC_000002.12:74910289:TTTTTTTTTTTT… NC_000002.12:74910289:TTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss3704203704	NC_000002.12:74910291:TT:	NC_000002.12:74910289:TTTTTTTTTTTT… NC_000002.12:74910289:TTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss103628334	NT_022184.15:53959316:TT:	NC_000002.12:74910289:TTTTTTTTTTTT… NC_000002.12:74910289:TTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss288180313	NC_000002.10:74990924:T:	NC_000002.12:74910289:TTTTTTTTTTTT… NC_000002.12:74910289:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss3728566499, ss5152088296, ss5820310316	NC_000002.11:75137416:T:	NC_000002.12:74910289:TTTTTTTTTTTT… NC_000002.12:74910289:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss1710009839, ss1710009840, ss3836937826	NC_000002.11:75137418:T:	NC_000002.12:74910289:TTTTTTTTTTTT… NC_000002.12:74910289:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss3801319646, ss4044144269, ss5248615323, ss5448765546, ss5680923652	NC_000002.12:74910289:T:	NC_000002.12:74910289:TTTTTTTTTTTT… NC_000002.12:74910289:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
3613201407	NC_000002.12:74910289:TTTTTTTTTTTT… NC_000002.12:74910289:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000002.12:74910289:TTTTTTTTTTTT… NC_000002.12:74910289:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss3842354003, ss3948068322	NC_000002.12:74910291:T:	NC_000002.12:74910289:TTTTTTTTTTTT… NC_000002.12:74910289:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss3704203705	NC_000002.12:74910292:T:	NC_000002.12:74910289:TTTTTTTTTTTT… NC_000002.12:74910289:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss41817331	NT_022184.15:53959305:T:	NC_000002.12:74910289:TTTTTTTTTTTT… NC_000002.12:74910289:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss3728566500, ss3827057821, ss5152088298	NC_000002.11:75137416::T	NC_000002.12:74910289:TTTTTTTTTTTT… NC_000002.12:74910289:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4044144265, ss5248615324, ss5448765547, ss5680923653	NC_000002.12:74910289::T	NC_000002.12:74910289:TTTTTTTTTTTT… NC_000002.12:74910289:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
3613201407	NC_000002.12:74910289:TTTTTTTTTTTT… NC_000002.12:74910289:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000002.12:74910289:TTTTTTTTTTTT… NC_000002.12:74910289:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3948068324	NC_000002.12:74910292::T	NC_000002.12:74910289:TTTTTTTTTTTT… NC_000002.12:74910289:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3704203706	NC_000002.12:74910293::T	NC_000002.12:74910289:TTTTTTTTTTTT… NC_000002.12:74910289:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss80183753	NT_022184.15:53959318::T	NC_000002.12:74910289:TTTTTTTTTTTT… NC_000002.12:74910289:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4044144266, ss5248615327	NC_000002.12:74910289::TT	NC_000002.12:74910289:TTTTTTTTTTTT… NC_000002.12:74910289:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
3613201407	NC_000002.12:74910289:TTTTTTTTTTTT… NC_000002.12:74910289:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000002.12:74910289:TTTTTTTTTTTT… NC_000002.12:74910289:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
3613201407	NC_000002.12:74910289:TTTTTTTTTTTT… NC_000002.12:74910289:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000002.12:74910289:TTTTTTTTTTTT… NC_000002.12:74910289:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4044144267	NC_000002.12:74910289::TTTTTTTTTTT… NC_000002.12:74910289::TTTTTTTTTTTTTTTT	NC_000002.12:74910289:TTTTTTTTTTTT… NC_000002.12:74910289:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(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 rs11343831

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

rs11343831