Name: rs11165012
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.

rs11165012

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr1:93825925 (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: T>C
Variation Type: SNV Single Nucleotide Variation
Frequency: C=0.193132 (58816/304538, ALFA)
C=0.337228 (89261/264690, TOPMED)
C=0.323850 (45306/139898, GnomAD) (+ 20 more)
C=0.42810 (33687/78690, PAGE_STUDY)
C=0.21054 (5949/28256, 14KJPN)
C=0.21295 (3569/16760, 8.3KJPN)
C=0.3682 (2358/6404, 1000G_30x)
C=0.3598 (1802/5008, 1000G)
C=0.1888 (846/4480, Estonian)
C=0.1645 (634/3854, ALSPAC)
C=0.1564 (580/3708, TWINSUK)
C=0.2038 (597/2930, KOREAN)
C=0.2961 (617/2084, HGDP_Stanford)
C=0.4376 (828/1892, HapMap)
C=0.2074 (380/1832, Korea1K)
C=0.147 (147/998, GoNL)
C=0.244 (189/774, PRJEB37584)
C=0.162 (97/600, NorthernSweden)
T=0.354 (95/268, SGDP_PRJ)
C=0.250 (54/216, Qatari)
C=0.33 (20/60, Ancient Sardinia)
C=0.10 (4/40, GENOME_DK)
T=0.46 (11/24, Siberian)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: BCAR3 : 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: 20230706150541

Population	Group	Sample Size	Ref Allele	Alt Allele
Total	Global	304538	T=0.806868	C=0.193132
European	Sub	269638	T=0.824617	C=0.175383
African	Sub	8382	T=0.3584	C=0.6416
African Others	Sub	318	T=0.239	C=0.761
African American	Sub	8064	T=0.3631	C=0.6369
Asian	Sub	3898	T=0.7917	C=0.2083
East Asian	Sub	3156	T=0.7887	C=0.2113
Other Asian	Sub	742	T=0.805	C=0.195
Latin American 1	Sub	1132	T=0.6837	C=0.3163
Latin American 2	Sub	7216	T=0.7470	C=0.2530
South Asian	Sub	5224	T=0.8086	C=0.1914
Other	Sub	9048	T=0.7622	C=0.2378

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	304538	T=0.806868	C=0.193132
Allele Frequency Aggregator	European	Sub	269638	T=0.824617	C=0.175383
Allele Frequency Aggregator	Other	Sub	9048	T=0.7622	C=0.2378
Allele Frequency Aggregator	African	Sub	8382	T=0.3584	C=0.6416
Allele Frequency Aggregator	Latin American 2	Sub	7216	T=0.7470	C=0.2530
Allele Frequency Aggregator	South Asian	Sub	5224	T=0.8086	C=0.1914
Allele Frequency Aggregator	Asian	Sub	3898	T=0.7917	C=0.2083
Allele Frequency Aggregator	Latin American 1	Sub	1132	T=0.6837	C=0.3163
TopMed	Global	Study-wide	264690	T=0.662772	C=0.337228
gnomAD - Genomes	Global	Study-wide	139898	T=0.676150	C=0.323850
gnomAD - Genomes	European	Sub	75868	T=0.83044	C=0.16956
gnomAD - Genomes	African	Sub	41810	T=0.36034	C=0.63966
gnomAD - Genomes	American	Sub	13630	T=0.73720	C=0.26280
gnomAD - Genomes	Ashkenazi Jewish	Sub	3324	T=0.8045	C=0.1955
gnomAD - Genomes	East Asian	Sub	3116	T=0.7397	C=0.2603
gnomAD - Genomes	Other	Sub	2150	T=0.6953	C=0.3047
The PAGE Study	Global	Study-wide	78690	T=0.57190	C=0.42810
The PAGE Study	AfricanAmerican	Sub	32514	T=0.36916	C=0.63084
The PAGE Study	Mexican	Sub	10808	T=0.75990	C=0.24010
The PAGE Study	Asian	Sub	8316	T=0.7730	C=0.2270
The PAGE Study	PuertoRican	Sub	7918	T=0.6831	C=0.3169
The PAGE Study	NativeHawaiian	Sub	4532	T=0.6516	C=0.3484
The PAGE Study	Cuban	Sub	4226	T=0.7404	C=0.2596
The PAGE Study	Dominican	Sub	3828	T=0.5697	C=0.4303
The PAGE Study	CentralAmerican	Sub	2450	T=0.6502	C=0.3498
The PAGE Study	SouthAmerican	Sub	1982	T=0.7407	C=0.2593
The PAGE Study	NativeAmerican	Sub	1260	T=0.7579	C=0.2421
The PAGE Study	SouthAsian	Sub	856	T=0.784	C=0.216
14KJPN	JAPANESE	Study-wide	28256	T=0.78946	C=0.21054
8.3KJPN	JAPANESE	Study-wide	16760	T=0.78705	C=0.21295
1000Genomes_30x	Global	Study-wide	6404	T=0.6318	C=0.3682
1000Genomes_30x	African	Sub	1786	T=0.2458	C=0.7542
1000Genomes_30x	Europe	Sub	1266	T=0.8254	C=0.1746
1000Genomes_30x	South Asian	Sub	1202	T=0.8178	C=0.1822
1000Genomes_30x	East Asian	Sub	1170	T=0.7479	C=0.2521
1000Genomes_30x	American	Sub	980	T=0.718	C=0.282
1000Genomes	Global	Study-wide	5008	T=0.6402	C=0.3598
1000Genomes	African	Sub	1322	T=0.2534	C=0.7466
1000Genomes	East Asian	Sub	1008	T=0.7480	C=0.2520
1000Genomes	Europe	Sub	1006	T=0.8221	C=0.1779
1000Genomes	South Asian	Sub	978	T=0.810	C=0.190
1000Genomes	American	Sub	694	T=0.718	C=0.282
Genetic variation in the Estonian population	Estonian	Study-wide	4480	T=0.8112	C=0.1888
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	T=0.8355	C=0.1645
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	T=0.8436	C=0.1564
KOREAN population from KRGDB	KOREAN	Study-wide	2930	T=0.7962	C=0.2038
HGDP-CEPH-db Supplement 1	Global	Study-wide	2084	T=0.7039	C=0.2961
HGDP-CEPH-db Supplement 1	Est_Asia	Sub	470	T=0.781	C=0.219
HGDP-CEPH-db Supplement 1	Central_South_Asia	Sub	414	T=0.790	C=0.210
HGDP-CEPH-db Supplement 1	Middle_Est	Sub	350	T=0.766	C=0.234
HGDP-CEPH-db Supplement 1	Europe	Sub	320	T=0.806	C=0.194
HGDP-CEPH-db Supplement 1	Africa	Sub	242	T=0.236	C=0.764
HGDP-CEPH-db Supplement 1	America	Sub	216	T=0.699	C=0.301
HGDP-CEPH-db Supplement 1	Oceania	Sub	72	T=0.54	C=0.46
HapMap	Global	Study-wide	1892	T=0.5624	C=0.4376
HapMap	American	Sub	770	T=0.749	C=0.251
HapMap	African	Sub	692	T=0.250	C=0.750
HapMap	Asian	Sub	254	T=0.685	C=0.315
HapMap	Europe	Sub	176	T=0.795	C=0.205
Korean Genome Project	KOREAN	Study-wide	1832	T=0.7926	C=0.2074
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	T=0.853	C=0.147
CNV burdens in cranial meningiomas	Global	Study-wide	774	T=0.756	C=0.244
CNV burdens in cranial meningiomas	CRM	Sub	774	T=0.756	C=0.244
Northern Sweden	ACPOP	Study-wide	600	T=0.838	C=0.162
SGDP_PRJ	Global	Study-wide	268	T=0.354	C=0.646
Qatari	Global	Study-wide	216	T=0.750	C=0.250
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	60	T=0.67	C=0.33
The Danish reference pan genome	Danish	Study-wide	40	T=0.90	C=0.10
Siberian	Global	Study-wide	24	T=0.46	C=0.54

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 1	NC_000001.11:g.93825925T>C
GRCh37.p13 chr 1	NC_000001.10:g.94291481T>C

Gene: BCAR3, BCAR3 adaptor protein, NSP family member (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
BCAR3 transcript variant 1	NM_001261408.2:c.-63+1964… NM_001261408.2:c.-63+19642A>G	N/A	Intron Variant
BCAR3 transcript variant 3	NM_001261409.1:c.	N/A	Genic Upstream Transcript Variant
BCAR3 transcript variant 4	NM_001261410.2:c.	N/A	Genic Upstream Transcript Variant
BCAR3 transcript variant 5	NM_001308251.1:c.	N/A	Genic Upstream Transcript Variant
BCAR3 transcript variant 2	NM_003567.4:c.	N/A	Genic Upstream Transcript Variant
BCAR3 transcript variant 6	NR_171551.1: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=	C
GRCh38.p14 chr 1	NC_000001.11:g.93825925=	NC_000001.11:g.93825925T>C
GRCh37.p13 chr 1	NC_000001.10:g.94291481=	NC_000001.10:g.94291481T>C
BCAR3 transcript variant 1	NM_001261408.1:c.-63+19642=	NM_001261408.1:c.-63+19642A>G
BCAR3 transcript variant 1	NM_001261408.2:c.-63+19642=	NM_001261408.2:c.-63+19642A>G

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#.

126 SubSNP, 23 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	CSHL-HAPMAP	ss17373103	Feb 27, 2004 (120)
2	SC_SNP	ss18293037	Feb 27, 2004 (120)
3	ILLUMINA	ss66924694	Nov 30, 2006 (127)
4	ILLUMINA	ss67074846	Nov 30, 2006 (127)
5	ILLUMINA	ss68102518	Dec 12, 2006 (127)
6	ILLUMINA	ss70522581	May 24, 2008 (130)
7	ILLUMINA	ss71051875	May 17, 2007 (127)
8	ILLUMINA	ss75648798	Dec 06, 2007 (129)
9	HGSV	ss78967815	Dec 06, 2007 (129)
10	HGSV	ss83657669	Dec 15, 2007 (130)
11	KRIBB_YJKIM	ss85080861	Dec 15, 2007 (130)
12	BCMHGSC_JDW	ss87631863	Mar 23, 2008 (129)
13	BGI	ss102763811	Dec 01, 2009 (131)
14	1000GENOMES	ss108420557	Jan 23, 2009 (130)
15	1000GENOMES	ss110836061	Jan 25, 2009 (130)
16	ILLUMINA-UK	ss118895494	Feb 14, 2009 (130)
17	ENSEMBL	ss138038595	Dec 01, 2009 (131)
18	ILLUMINA	ss152952920	Dec 01, 2009 (131)
19	ILLUMINA	ss159168317	Dec 01, 2009 (131)
20	ILLUMINA	ss159965417	Dec 01, 2009 (131)
21	COMPLETE_GENOMICS	ss163676009	Jul 04, 2010 (132)
22	ILLUMINA	ss171113295	Jul 04, 2010 (132)
23	BUSHMAN	ss198786900	Jul 04, 2010 (132)
24	BCM-HGSC-SUB	ss205381235	Jul 04, 2010 (132)
25	1000GENOMES	ss218528528	Jul 14, 2010 (132)
26	1000GENOMES	ss230641011	Jul 14, 2010 (132)
27	1000GENOMES	ss238311919	Jul 15, 2010 (132)
28	GMI	ss275930767	May 04, 2012 (137)
29	GMI	ss284098857	Apr 25, 2013 (138)
30	ILLUMINA	ss479484621	May 04, 2012 (137)
31	ILLUMINA	ss479488621	May 04, 2012 (137)
32	ILLUMINA	ss479927458	Sep 08, 2015 (146)
33	ILLUMINA	ss484541841	May 04, 2012 (137)
34	ILLUMINA	ss536681918	Sep 08, 2015 (146)
35	TISHKOFF	ss554440222	Apr 25, 2013 (138)
36	SSMP	ss648226512	Apr 25, 2013 (138)
37	ILLUMINA	ss778379395	Sep 08, 2015 (146)
38	ILLUMINA	ss782717555	Sep 08, 2015 (146)
39	ILLUMINA	ss783685192	Sep 08, 2015 (146)
40	ILLUMINA	ss831969046	Sep 08, 2015 (146)
41	ILLUMINA	ss832680868	Jul 12, 2019 (153)
42	ILLUMINA	ss833834362	Sep 08, 2015 (146)
43	EVA-GONL	ss975440525	Aug 21, 2014 (142)
44	JMKIDD_LAB	ss1068097407	Aug 21, 2014 (142)
45	1000GENOMES	ss1291950248	Aug 21, 2014 (142)
46	DDI	ss1425899553	Apr 01, 2015 (144)
47	EVA_GENOME_DK	ss1574238890	Apr 01, 2015 (144)
48	EVA_DECODE	ss1584817375	Apr 01, 2015 (144)
49	EVA_UK10K_ALSPAC	ss1600730819	Apr 01, 2015 (144)
50	EVA_UK10K_TWINSUK	ss1643724852	Apr 01, 2015 (144)
51	EVA_SVP	ss1712353874	Apr 01, 2015 (144)
52	ILLUMINA	ss1751939342	Sep 08, 2015 (146)
53	HAMMER_LAB	ss1794753349	Sep 08, 2015 (146)
54	WEILL_CORNELL_DGM	ss1918641351	Feb 12, 2016 (147)
55	ILLUMINA	ss1946001902	Feb 12, 2016 (147)
56	ILLUMINA	ss1958293959	Feb 12, 2016 (147)
57	GENOMED	ss1966810987	Jul 19, 2016 (147)
58	JJLAB	ss2019842112	Sep 14, 2016 (149)
59	USC_VALOUEV	ss2147860283	Dec 20, 2016 (150)
60	HUMAN_LONGEVITY	ss2164693072	Dec 20, 2016 (150)
61	SYSTEMSBIOZJU	ss2624432495	Nov 08, 2017 (151)
62	ILLUMINA	ss2632548463	Nov 08, 2017 (151)
63	GRF	ss2697786492	Nov 08, 2017 (151)
64	ILLUMINA	ss2710677474	Nov 08, 2017 (151)
65	GNOMAD	ss2758181997	Nov 08, 2017 (151)
66	SWEGEN	ss2987242671	Nov 08, 2017 (151)
67	ILLUMINA	ss3021110559	Nov 08, 2017 (151)
68	BIOINF_KMB_FNS_UNIBA	ss3023684031	Nov 08, 2017 (151)
69	CSHL	ss3343577635	Nov 08, 2017 (151)
70	ILLUMINA	ss3625545384	Oct 11, 2018 (152)
71	ILLUMINA	ss3626156429	Oct 11, 2018 (152)
72	ILLUMINA	ss3630582897	Oct 11, 2018 (152)
73	ILLUMINA	ss3632901257	Oct 11, 2018 (152)
74	ILLUMINA	ss3633596182	Oct 11, 2018 (152)
75	ILLUMINA	ss3634336921	Oct 11, 2018 (152)
76	ILLUMINA	ss3635289844	Oct 11, 2018 (152)
77	ILLUMINA	ss3636014326	Oct 11, 2018 (152)
78	ILLUMINA	ss3637040291	Oct 11, 2018 (152)
79	ILLUMINA	ss3637772589	Oct 11, 2018 (152)
80	ILLUMINA	ss3638904787	Oct 11, 2018 (152)
81	ILLUMINA	ss3639764598	Oct 11, 2018 (152)
82	ILLUMINA	ss3640044281	Oct 11, 2018 (152)
83	ILLUMINA	ss3640984156	Oct 11, 2018 (152)
84	ILLUMINA	ss3641278139	Oct 11, 2018 (152)
85	ILLUMINA	ss3642783104	Oct 11, 2018 (152)
86	ILLUMINA	ss3643818174	Oct 11, 2018 (152)
87	ILLUMINA	ss3644497861	Oct 11, 2018 (152)
88	ILLUMINA	ss3651441080	Oct 11, 2018 (152)
89	EGCUT_WGS	ss3655321851	Jul 12, 2019 (153)
90	EVA_DECODE	ss3687290245	Jul 12, 2019 (153)
91	ILLUMINA	ss3725045201	Jul 12, 2019 (153)
92	ACPOP	ss3727279306	Jul 12, 2019 (153)
93	ILLUMINA	ss3744050352	Jul 12, 2019 (153)
94	ILLUMINA	ss3744637881	Jul 12, 2019 (153)
95	EVA	ss3746525984	Jul 12, 2019 (153)
96	PAGE_CC	ss3770825725	Jul 12, 2019 (153)
97	ILLUMINA	ss3772139147	Jul 12, 2019 (153)
98	PACBIO	ss3783485356	Jul 12, 2019 (153)
99	PACBIO	ss3789131959	Jul 12, 2019 (153)
100	PACBIO	ss3794004784	Jul 12, 2019 (153)
101	KHV_HUMAN_GENOMES	ss3799529189	Jul 12, 2019 (153)
102	EVA	ss3826307153	Apr 25, 2020 (154)
103	HGDP	ss3847342458	Apr 25, 2020 (154)
104	SGDP_PRJ	ss3849397474	Apr 25, 2020 (154)
105	KRGDB	ss3894466501	Apr 25, 2020 (154)
106	KOGIC	ss3945018000	Apr 25, 2020 (154)
107	EVA	ss3984461100	Apr 25, 2021 (155)
108	EVA	ss3984812671	Apr 25, 2021 (155)
109	EVA	ss4016925109	Apr 25, 2021 (155)
110	TOPMED	ss4459248539	Apr 25, 2021 (155)
111	TOMMO_GENOMICS	ss5145136829	Apr 25, 2021 (155)
112	1000G_HIGH_COVERAGE	ss5243187510	Oct 12, 2022 (156)
113	EVA	ss5314634982	Oct 12, 2022 (156)
114	EVA	ss5320418670	Oct 12, 2022 (156)
115	HUGCELL_USP	ss5444152487	Oct 12, 2022 (156)
116	EVA	ss5505949884	Oct 12, 2022 (156)
117	1000G_HIGH_COVERAGE	ss5515953292	Oct 12, 2022 (156)
118	SANFORD_IMAGENETICS	ss5626056021	Oct 12, 2022 (156)
119	TOMMO_GENOMICS	ss5670246832	Oct 12, 2022 (156)
120	EVA	ss5799492029	Oct 12, 2022 (156)
121	YY_MCH	ss5800826569	Oct 12, 2022 (156)
122	EVA	ss5832318347	Oct 12, 2022 (156)
123	EVA	ss5847547275	Oct 12, 2022 (156)
124	EVA	ss5849017649	Oct 12, 2022 (156)
125	EVA	ss5909316135	Oct 12, 2022 (156)
126	EVA	ss5937910877	Oct 12, 2022 (156)
127	1000Genomes	NC_000001.10 - 94291481	Oct 11, 2018 (152)
128	1000Genomes_30x	NC_000001.11 - 93825925	Oct 12, 2022 (156)
129	The Avon Longitudinal Study of Parents and Children	NC_000001.10 - 94291481	Oct 11, 2018 (152)
130	Genetic variation in the Estonian population	NC_000001.10 - 94291481	Oct 11, 2018 (152)
131	The Danish reference pan genome	NC_000001.10 - 94291481	Apr 25, 2020 (154)
132	gnomAD - Genomes	NC_000001.11 - 93825925	Apr 25, 2021 (155)
133	Genome of the Netherlands Release 5	NC_000001.10 - 94291481	Apr 25, 2020 (154)
134	HGDP-CEPH-db Supplement 1	NC_000001.9 - 94064069	Apr 25, 2020 (154)
135	HapMap	NC_000001.11 - 93825925	Apr 25, 2020 (154)
136	KOREAN population from KRGDB	NC_000001.10 - 94291481	Apr 25, 2020 (154)
137	Korean Genome Project	NC_000001.11 - 93825925	Apr 25, 2020 (154)
138	Northern Sweden	NC_000001.10 - 94291481	Jul 12, 2019 (153)
139	The PAGE Study	NC_000001.11 - 93825925	Jul 12, 2019 (153)
140	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000001.10 - 94291481	Apr 25, 2021 (155)
141	CNV burdens in cranial meningiomas	NC_000001.10 - 94291481	Apr 25, 2021 (155)
142	Qatari	NC_000001.10 - 94291481	Apr 25, 2020 (154)
143	SGDP_PRJ	NC_000001.10 - 94291481	Apr 25, 2020 (154)
144	Siberian	NC_000001.10 - 94291481	Apr 25, 2020 (154)
145	8.3KJPN	NC_000001.10 - 94291481	Apr 25, 2021 (155)
146	14KJPN	NC_000001.11 - 93825925	Oct 12, 2022 (156)
147	TopMed	NC_000001.11 - 93825925	Apr 25, 2021 (155)
148	UK 10K study - Twins	NC_000001.10 - 94291481	Oct 11, 2018 (152)
149	ALFA	NC_000001.11 - 93825925	Apr 25, 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)
rs58386567	May 24, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss78967815, ss83657669, ss3638904787, ss3639764598, ss3643818174	NC_000001.8:94003501:T:C	NC_000001.11:93825924:T:C	(self)
20350, ss87631863, ss108420557, ss110836061, ss118895494, ss163676009, ss198786900, ss205381235, ss275930767, ss284098857, ss479484621, ss1584817375, ss1712353874, ss3642783104, ss3847342458	NC_000001.9:94064068:T:C	NC_000001.11:93825924:T:C	(self)
2708356, 1489709, 1060099, 1612016, 645456, 1643895, 564171, 38598, 10411, 683281, 1414454, 376637, 3106136, 1489709, ss218528528, ss230641011, ss238311919, ss479488621, ss479927458, ss484541841, ss536681918, ss554440222, ss648226512, ss778379395, ss782717555, ss783685192, ss831969046, ss832680868, ss833834362, ss975440525, ss1068097407, ss1291950248, ss1425899553, ss1574238890, ss1600730819, ss1643724852, ss1751939342, ss1794753349, ss1918641351, ss1946001902, ss1958293959, ss1966810987, ss2019842112, ss2147860283, ss2624432495, ss2632548463, ss2697786492, ss2710677474, ss2758181997, ss2987242671, ss3021110559, ss3343577635, ss3625545384, ss3626156429, ss3630582897, ss3632901257, ss3633596182, ss3634336921, ss3635289844, ss3636014326, ss3637040291, ss3637772589, ss3640044281, ss3640984156, ss3641278139, ss3644497861, ss3651441080, ss3655321851, ss3727279306, ss3744050352, ss3744637881, ss3746525984, ss3772139147, ss3783485356, ss3789131959, ss3794004784, ss3826307153, ss3849397474, ss3894466501, ss3984461100, ss3984812671, ss4016925109, ss5145136829, ss5314634982, ss5320418670, ss5505949884, ss5626056021, ss5799492029, ss5832318347, ss5847547275, ss5937910877	NC_000001.10:94291480:T:C	NC_000001.11:93825924:T:C	(self)
3479227, 19129182, 128180, 1396001, 47194, 4083936, 22854874, 2236694483, ss2164693072, ss3023684031, ss3687290245, ss3725045201, ss3770825725, ss3799529189, ss3945018000, ss4459248539, ss5243187510, ss5444152487, ss5515953292, ss5670246832, ss5800826569, ss5849017649, ss5909316135	NC_000001.11:93825924:T:C	NC_000001.11:93825924:T:C	(self)
ss17373103, ss18293037	NT_028050.13:2489302:T:C	NC_000001.11:93825924:T:C	(self)
ss66924694, ss67074846, ss68102518, ss70522581, ss71051875, ss75648798, ss85080861, ss102763811, ss138038595, ss152952920, ss159168317, ss159965417, ss171113295	NT_032977.9:64263398:T:C	NC_000001.11:93825924:T:C	(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 rs11165012

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

rs11165012