Name: rs11893367
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.

rs11893367

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr2:29367044 (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: C>T
Variation Type: SNV Single Nucleotide Variation
Frequency: T=0.151955 (40221/264690, TOPMED)
T=0.136600 (27696/202752, ALFA)
T=0.154906 (21680/139956, GnomAD) (+ 21 more)
T=0.15520 (12214/78696, PAGE_STUDY)
T=0.09272 (2620/28258, 14KJPN)
T=0.09117 (1528/16760, 8.3KJPN)
T=0.1507 (965/6404, 1000G_30x)
T=0.1508 (755/5008, 1000G)
T=0.1027 (460/4480, Estonian)
T=0.1422 (548/3854, ALSPAC)
T=0.1281 (475/3708, TWINSUK)
T=0.1362 (398/2922, KOREAN)
T=0.1051 (219/2084, HGDP_Stanford)
T=0.1735 (328/1890, HapMap)
T=0.1146 (210/1832, Korea1K)
T=0.1384 (157/1134, Daghestan)
T=0.124 (124/998, GoNL)
T=0.155 (93/600, NorthernSweden)
T=0.116 (25/216, Qatari)
T=0.093 (20/216, Vietnamese)
C=0.483 (56/116, SGDP_PRJ)
T=0.31 (16/52, Ancient Sardinia)
T=0.17 (7/40, GENOME_DK)
C=0.42 (5/12, Siberian)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: ALK : 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	202752	C=0.863400	T=0.136600
European	Sub	174876	C=0.863412	T=0.136588
African	Sub	7498	C=0.8089	T=0.1911
African Others	Sub	264	C=0.822	T=0.178
African American	Sub	7234	C=0.8084	T=0.1916
Asian	Sub	734	C=0.857	T=0.143
East Asian	Sub	588	C=0.864	T=0.136
Other Asian	Sub	146	C=0.829	T=0.171
Latin American 1	Sub	838	C=0.853	T=0.147
Latin American 2	Sub	6886	C=0.9201	T=0.0799
South Asian	Sub	5048	C=0.8645	T=0.1355
Other	Sub	6872	C=0.8669	T=0.1331

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
TopMed	Global	Study-wide	264690	C=0.848045	T=0.151955
Allele Frequency Aggregator	Total	Global	202752	C=0.863400	T=0.136600
Allele Frequency Aggregator	European	Sub	174876	C=0.863412	T=0.136588
Allele Frequency Aggregator	African	Sub	7498	C=0.8089	T=0.1911
Allele Frequency Aggregator	Latin American 2	Sub	6886	C=0.9201	T=0.0799
Allele Frequency Aggregator	Other	Sub	6872	C=0.8669	T=0.1331
Allele Frequency Aggregator	South Asian	Sub	5048	C=0.8645	T=0.1355
Allele Frequency Aggregator	Latin American 1	Sub	838	C=0.853	T=0.147
Allele Frequency Aggregator	Asian	Sub	734	C=0.857	T=0.143
gnomAD - Genomes	Global	Study-wide	139956	C=0.845094	T=0.154906
gnomAD - Genomes	European	Sub	75826	C=0.86133	T=0.13867
gnomAD - Genomes	African	Sub	41900	C=0.79811	T=0.20189
gnomAD - Genomes	American	Sub	13630	C=0.88855	T=0.11145
gnomAD - Genomes	Ashkenazi Jewish	Sub	3322	C=0.8703	T=0.1297
gnomAD - Genomes	East Asian	Sub	3128	C=0.8558	T=0.1442
gnomAD - Genomes	Other	Sub	2150	C=0.8581	T=0.1419
The PAGE Study	Global	Study-wide	78696	C=0.84480	T=0.15520
The PAGE Study	AfricanAmerican	Sub	32514	C=0.79978	T=0.20022
The PAGE Study	Mexican	Sub	10810	C=0.91804	T=0.08196
The PAGE Study	Asian	Sub	8316	C=0.8929	T=0.1071
The PAGE Study	PuertoRican	Sub	7918	C=0.8479	T=0.1521
The PAGE Study	NativeHawaiian	Sub	4534	C=0.8368	T=0.1632
The PAGE Study	Cuban	Sub	4230	C=0.8423	T=0.1577
The PAGE Study	Dominican	Sub	3826	C=0.8309	T=0.1691
The PAGE Study	CentralAmerican	Sub	2450	C=0.9016	T=0.0984
The PAGE Study	SouthAmerican	Sub	1982	C=0.9284	T=0.0716
The PAGE Study	NativeAmerican	Sub	1260	C=0.8722	T=0.1278
The PAGE Study	SouthAsian	Sub	856	C=0.854	T=0.146
14KJPN	JAPANESE	Study-wide	28258	C=0.90728	T=0.09272
8.3KJPN	JAPANESE	Study-wide	16760	C=0.90883	T=0.09117
1000Genomes_30x	Global	Study-wide	6404	C=0.8493	T=0.1507
1000Genomes_30x	African	Sub	1786	C=0.7900	T=0.2100
1000Genomes_30x	Europe	Sub	1266	C=0.8626	T=0.1374
1000Genomes_30x	South Asian	Sub	1202	C=0.8694	T=0.1306
1000Genomes_30x	East Asian	Sub	1170	C=0.8513	T=0.1487
1000Genomes_30x	American	Sub	980	C=0.913	T=0.087
1000Genomes	Global	Study-wide	5008	C=0.8492	T=0.1508
1000Genomes	African	Sub	1322	C=0.7943	T=0.2057
1000Genomes	East Asian	Sub	1008	C=0.8482	T=0.1518
1000Genomes	Europe	Sub	1006	C=0.8658	T=0.1342
1000Genomes	South Asian	Sub	978	C=0.866	T=0.134
1000Genomes	American	Sub	694	C=0.908	T=0.092
Genetic variation in the Estonian population	Estonian	Study-wide	4480	C=0.8973	T=0.1027
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	C=0.8578	T=0.1422
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	C=0.8719	T=0.1281
KOREAN population from KRGDB	KOREAN	Study-wide	2922	C=0.8638	T=0.1362
HGDP-CEPH-db Supplement 1	Global	Study-wide	2084	C=0.8949	T=0.1051
HGDP-CEPH-db Supplement 1	Est_Asia	Sub	470	C=0.885	T=0.115
HGDP-CEPH-db Supplement 1	Central_South_Asia	Sub	414	C=0.882	T=0.118
HGDP-CEPH-db Supplement 1	Middle_Est	Sub	350	C=0.869	T=0.131
HGDP-CEPH-db Supplement 1	Europe	Sub	320	C=0.875	T=0.125
HGDP-CEPH-db Supplement 1	Africa	Sub	242	C=0.880	T=0.120
HGDP-CEPH-db Supplement 1	America	Sub	216	C=0.995	T=0.005
HGDP-CEPH-db Supplement 1	Oceania	Sub	72	C=1.00	T=0.00
HapMap	Global	Study-wide	1890	C=0.8265	T=0.1735
HapMap	American	Sub	768	C=0.854	T=0.146
HapMap	African	Sub	692	C=0.762	T=0.238
HapMap	Asian	Sub	254	C=0.890	T=0.110
HapMap	Europe	Sub	176	C=0.869	T=0.131
Korean Genome Project	KOREAN	Study-wide	1832	C=0.8854	T=0.1146
Genome-wide autozygosity in Daghestan	Global	Study-wide	1134	C=0.8616	T=0.1384
Genome-wide autozygosity in Daghestan	Daghestan	Sub	626	C=0.835	T=0.165
Genome-wide autozygosity in Daghestan	Near_East	Sub	144	C=0.931	T=0.069
Genome-wide autozygosity in Daghestan	Central Asia	Sub	122	C=0.918	T=0.082
Genome-wide autozygosity in Daghestan	Europe	Sub	108	C=0.861	T=0.139
Genome-wide autozygosity in Daghestan	South Asian	Sub	98	C=0.86	T=0.14
Genome-wide autozygosity in Daghestan	Caucasus	Sub	36	C=0.86	T=0.14
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	C=0.876	T=0.124
Northern Sweden	ACPOP	Study-wide	600	C=0.845	T=0.155
Qatari	Global	Study-wide	216	C=0.884	T=0.116
A Vietnamese Genetic Variation Database	Global	Study-wide	216	C=0.907	T=0.093
SGDP_PRJ	Global	Study-wide	116	C=0.483	T=0.517
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	52	C=0.69	T=0.31
The Danish reference pan genome	Danish	Study-wide	40	C=0.82	T=0.17
Siberian	Global	Study-wide	12	C=0.42	T=0.58

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.29367044C>T
GRCh37.p13 chr 2	NC_000002.11:g.29589910C>T
ALK RefSeqGene (LRG_488)	NG_009445.1:g.559523G>A

Gene: ALK, ALK receptor tyrosine kinase (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
ALK transcript variant 1	NM_004304.5:c.1282+16688G… NM_004304.5:c.1282+16688G>A	N/A	Intron Variant
ALK transcript variant 2	NM_001353765.2:c.	N/A	Genic Upstream Transcript Variant
ALK transcript variant X1	XR_001738688.3: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	C=	T
GRCh38.p14 chr 2	NC_000002.12:g.29367044=	NC_000002.12:g.29367044C>T
GRCh37.p13 chr 2	NC_000002.11:g.29589910=	NC_000002.11:g.29589910C>T
ALK RefSeqGene (LRG_488)	NG_009445.1:g.559523=	NG_009445.1:g.559523G>A
ALK transcript variant 1	NM_004304.4:c.1282+16688=	NM_004304.4:c.1282+16688G>A
ALK transcript variant 1	NM_004304.5:c.1282+16688=	NM_004304.5:c.1282+16688G>A

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#.

120 SubSNP, 24 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	CSHL-HAPMAP	ss17655009	Feb 28, 2004 (120)
2	ABI	ss44174771	Mar 14, 2006 (126)
3	ILLUMINA	ss66668980	Dec 01, 2006 (127)
4	ILLUMINA	ss66965463	Dec 01, 2006 (127)
5	ILLUMINA	ss67132410	Dec 01, 2006 (127)
6	ILLUMINA	ss70401735	May 17, 2007 (127)
7	ILLUMINA	ss70547103	May 24, 2008 (130)
8	ILLUMINA	ss71081071	May 17, 2007 (127)
9	ILLUMINA	ss75554409	Dec 07, 2007 (129)
10	HGSV	ss77762811	Dec 07, 2007 (129)
11	HGSV	ss84994639	Dec 14, 2007 (130)
12	KRIBB_YJKIM	ss85156650	Dec 14, 2007 (130)
13	1000GENOMES	ss109360853	Jan 24, 2009 (130)
14	1000GENOMES	ss110002849	Jan 24, 2009 (130)
15	ILLUMINA	ss121517312	Dec 01, 2009 (131)
16	ILLUMINA	ss153086175	Dec 01, 2009 (131)
17	ILLUMINA	ss159194669	Dec 01, 2009 (131)
18	ILLUMINA	ss160014835	Dec 01, 2009 (131)
19	ENSEMBL	ss161256147	Dec 01, 2009 (131)
20	COMPLETE_GENOMICS	ss163233341	Jul 04, 2010 (132)
21	COMPLETE_GENOMICS	ss164073598	Jul 04, 2010 (132)
22	ILLUMINA	ss169990159	Jul 04, 2010 (132)
23	ILLUMINA	ss171691190	Jul 04, 2010 (132)
24	1000GENOMES	ss219140921	Jul 14, 2010 (132)
25	1000GENOMES	ss231091222	Jul 14, 2010 (132)
26	1000GENOMES	ss238663465	Jul 15, 2010 (132)
27	GMI	ss276398877	May 04, 2012 (137)
28	PJP	ss292534468	May 09, 2011 (134)
29	ILLUMINA	ss479621870	May 04, 2012 (137)
30	ILLUMINA	ss479627161	May 04, 2012 (137)
31	ILLUMINA	ss480125032	Sep 08, 2015 (146)
32	ILLUMINA	ss484609691	May 04, 2012 (137)
33	ILLUMINA	ss536734613	Sep 08, 2015 (146)
34	TISHKOFF	ss555440814	Apr 25, 2013 (138)
35	SSMP	ss649021188	Apr 25, 2013 (138)
36	ILLUMINA	ss778394282	Sep 08, 2015 (146)
37	ILLUMINA	ss782751661	Sep 08, 2015 (146)
38	ILLUMINA	ss783718304	Sep 08, 2015 (146)
39	ILLUMINA	ss825371043	Apr 01, 2015 (144)
40	ILLUMINA	ss832003792	Sep 08, 2015 (146)
41	ILLUMINA	ss832707141	Jul 13, 2019 (153)
42	ILLUMINA	ss833849380	Sep 08, 2015 (146)
43	EVA-GONL	ss976627874	Aug 21, 2014 (142)
44	JMKIDD_LAB	ss1068962230	Aug 21, 2014 (142)
45	1000GENOMES	ss1296449245	Aug 21, 2014 (142)
46	HAMMER_LAB	ss1397286199	Sep 08, 2015 (146)
47	EVA_GENOME_DK	ss1578795669	Apr 01, 2015 (144)
48	EVA_DECODE	ss1586033801	Apr 01, 2015 (144)
49	EVA_UK10K_ALSPAC	ss1603096576	Apr 01, 2015 (144)
50	EVA_UK10K_TWINSUK	ss1646090609	Apr 01, 2015 (144)
51	EVA_SVP	ss1712441199	Apr 01, 2015 (144)
52	ILLUMINA	ss1752351607	Sep 08, 2015 (146)
53	HAMMER_LAB	ss1796473413	Sep 08, 2015 (146)
54	WEILL_CORNELL_DGM	ss1919860228	Feb 12, 2016 (147)
55	ILLUMINA	ss1958402250	Feb 12, 2016 (147)
56	JJLAB	ss2020458775	Sep 14, 2016 (149)
57	ILLUMINA	ss2095088948	Dec 20, 2016 (150)
58	USC_VALOUEV	ss2148503325	Dec 20, 2016 (150)
59	HUMAN_LONGEVITY	ss2228640603	Dec 20, 2016 (150)
60	ILLUMINA	ss2633589363	Nov 08, 2017 (151)
61	GRF	ss2703064389	Nov 08, 2017 (151)
62	GNOMAD	ss2771252507	Nov 08, 2017 (151)
63	AFFY	ss2985787761	Nov 08, 2017 (151)
64	SWEGEN	ss2989193959	Nov 08, 2017 (151)
65	ILLUMINA	ss3021954575	Nov 08, 2017 (151)
66	BIOINF_KMB_FNS_UNIBA	ss3023995849	Nov 08, 2017 (151)
67	CSHL	ss3344136225	Nov 08, 2017 (151)
68	ILLUMINA	ss3628022200	Oct 11, 2018 (152)
69	ILLUMINA	ss3631557793	Oct 11, 2018 (152)
70	ILLUMINA	ss3633193444	Oct 11, 2018 (152)
71	ILLUMINA	ss3633904808	Oct 11, 2018 (152)
72	ILLUMINA	ss3634757803	Oct 11, 2018 (152)
73	ILLUMINA	ss3635591245	Oct 11, 2018 (152)
74	ILLUMINA	ss3636443465	Oct 11, 2018 (152)
75	ILLUMINA	ss3637343075	Oct 11, 2018 (152)
76	ILLUMINA	ss3638249773	Oct 11, 2018 (152)
77	ILLUMINA	ss3639129562	Oct 11, 2018 (152)
78	ILLUMINA	ss3639576234	Oct 11, 2018 (152)
79	ILLUMINA	ss3640465106	Oct 11, 2018 (152)
80	ILLUMINA	ss3643220687	Oct 11, 2018 (152)
81	ILLUMINA	ss3652384007	Oct 11, 2018 (152)
82	EGCUT_WGS	ss3657149324	Jul 13, 2019 (153)
83	EVA_DECODE	ss3703515454	Jul 13, 2019 (153)
84	ILLUMINA	ss3725769881	Jul 13, 2019 (153)
85	ACPOP	ss3728267889	Jul 13, 2019 (153)
86	ILLUMINA	ss3745057747	Jul 13, 2019 (153)
87	EVA	ss3756519890	Jul 13, 2019 (153)
88	PAGE_CC	ss3770906794	Jul 13, 2019 (153)
89	ILLUMINA	ss3772554614	Jul 13, 2019 (153)
90	KHV_HUMAN_GENOMES	ss3800899044	Jul 13, 2019 (153)
91	EVA	ss3826887481	Apr 25, 2020 (154)
92	EVA	ss3836850995	Apr 25, 2020 (154)
93	EVA	ss3842265670	Apr 25, 2020 (154)
94	HGDP	ss3847611075	Apr 25, 2020 (154)
95	SGDP_PRJ	ss3851869839	Apr 25, 2020 (154)
96	KRGDB	ss3897287642	Apr 25, 2020 (154)
97	KOGIC	ss3947382069	Apr 25, 2020 (154)
98	EVA	ss3984881580	Apr 26, 2021 (155)
99	EVA	ss4016986545	Apr 26, 2021 (155)
100	TOPMED	ss4498841295	Apr 26, 2021 (155)
101	TOMMO_GENOMICS	ss5150479711	Apr 26, 2021 (155)
102	EVA	ss5237290741	Apr 26, 2021 (155)
103	1000G_HIGH_COVERAGE	ss5247384956	Oct 17, 2022 (156)
104	EVA	ss5314720272	Oct 17, 2022 (156)
105	EVA	ss5327680087	Oct 17, 2022 (156)
106	HUGCELL_USP	ss5447650370	Oct 17, 2022 (156)
107	EVA	ss5506337294	Oct 17, 2022 (156)
108	1000G_HIGH_COVERAGE	ss5522246880	Oct 17, 2022 (156)
109	SANFORD_IMAGENETICS	ss5624440185	Oct 17, 2022 (156)
110	SANFORD_IMAGENETICS	ss5628358560	Oct 17, 2022 (156)
111	TOMMO_GENOMICS	ss5678850077	Oct 17, 2022 (156)
112	EVA	ss5799526074	Oct 17, 2022 (156)
113	YY_MCH	ss5802039266	Oct 17, 2022 (156)
114	EVA	ss5819836812	Oct 17, 2022 (156)
115	EVA	ss5847184350	Oct 17, 2022 (156)
116	EVA	ss5847861436	Oct 17, 2022 (156)
117	EVA	ss5852444464	Oct 17, 2022 (156)
118	EVA	ss5929573669	Oct 17, 2022 (156)
119	EVA	ss5954562666	Oct 17, 2022 (156)
120	EVA	ss5979560853	Oct 17, 2022 (156)
121	1000Genomes	NC_000002.11 - 29589910	Oct 11, 2018 (152)
122	1000Genomes_30x	NC_000002.12 - 29367044	Oct 17, 2022 (156)
123	The Avon Longitudinal Study of Parents and Children	NC_000002.11 - 29589910	Oct 11, 2018 (152)
124	Genome-wide autozygosity in Daghestan	NC_000002.10 - 29443414	Apr 25, 2020 (154)
125	Genetic variation in the Estonian population	NC_000002.11 - 29589910	Oct 11, 2018 (152)
126	The Danish reference pan genome	NC_000002.11 - 29589910	Apr 25, 2020 (154)
127	gnomAD - Genomes	NC_000002.12 - 29367044	Apr 26, 2021 (155)
128	Genome of the Netherlands Release 5	NC_000002.11 - 29589910	Apr 25, 2020 (154)
129	HGDP-CEPH-db Supplement 1	NC_000002.10 - 29443414	Apr 25, 2020 (154)
130	HapMap	NC_000002.12 - 29367044	Apr 25, 2020 (154)
131	KOREAN population from KRGDB	NC_000002.11 - 29589910	Apr 25, 2020 (154)
132	Korean Genome Project	NC_000002.12 - 29367044	Apr 25, 2020 (154)
133	Northern Sweden	NC_000002.11 - 29589910	Jul 13, 2019 (153)
134	The PAGE Study	NC_000002.12 - 29367044	Jul 13, 2019 (153)
135	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000002.11 - 29589910	Apr 26, 2021 (155)
136	Qatari	NC_000002.11 - 29589910	Apr 25, 2020 (154)
137	SGDP_PRJ	NC_000002.11 - 29589910	Apr 25, 2020 (154)
138	Siberian	NC_000002.11 - 29589910	Apr 25, 2020 (154)
139	8.3KJPN	NC_000002.11 - 29589910	Apr 26, 2021 (155)
140	14KJPN	NC_000002.12 - 29367044	Oct 17, 2022 (156)
141	TopMed	NC_000002.12 - 29367044	Apr 26, 2021 (155)
142	UK 10K study - Twins	NC_000002.11 - 29589910	Oct 11, 2018 (152)
143	A Vietnamese Genetic Variation Database	NC_000002.11 - 29589910	Jul 13, 2019 (153)
144	ALFA	NC_000002.12 - 29367044	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)
rs57777150	May 24, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss77762811, ss84994639, ss3639129562, ss3639576234	NC_000002.9:29501560:C:T	NC_000002.12:29367043:C:T	(self)
236373, 288967, ss109360853, ss110002849, ss163233341, ss164073598, ss276398877, ss292534468, ss479621870, ss825371043, ss1397286199, ss1586033801, ss1712441199, ss3643220687, ss3847611075	NC_000002.10:29443413:C:T	NC_000002.12:29367043:C:T	(self)
7369614, 4091506, 2887572, 4971553, 1796780, 4465036, 1552754, 107507, 1902158, 3886819, 1019679, 8449018, 4091506, 890659, ss219140921, ss231091222, ss238663465, ss479627161, ss480125032, ss484609691, ss536734613, ss555440814, ss649021188, ss778394282, ss782751661, ss783718304, ss832003792, ss832707141, ss833849380, ss976627874, ss1068962230, ss1296449245, ss1578795669, ss1603096576, ss1646090609, ss1752351607, ss1796473413, ss1919860228, ss1958402250, ss2020458775, ss2095088948, ss2148503325, ss2633589363, ss2703064389, ss2771252507, ss2985787761, ss2989193959, ss3021954575, ss3344136225, ss3628022200, ss3631557793, ss3633193444, ss3633904808, ss3634757803, ss3635591245, ss3636443465, ss3637343075, ss3638249773, ss3640465106, ss3652384007, ss3657149324, ss3728267889, ss3745057747, ss3756519890, ss3772554614, ss3826887481, ss3836850995, ss3851869839, ss3897287642, ss3984881580, ss4016986545, ss5150479711, ss5237290741, ss5314720272, ss5327680087, ss5506337294, ss5624440185, ss5628358560, ss5799526074, ss5819836812, ss5847184350, ss5847861436, ss5954562666, ss5979560853	NC_000002.11:29589909:C:T	NC_000002.12:29367043:C:T	(self)
9772815, 52367177, 1761029, 3760070, 128263, 12687181, 302664174, 11298502843, ss2228640603, ss3023995849, ss3703515454, ss3725769881, ss3770906794, ss3800899044, ss3842265670, ss3947382069, ss4498841295, ss5247384956, ss5447650370, ss5522246880, ss5678850077, ss5802039266, ss5852444464, ss5929573669	NC_000002.12:29367043:C:T	NC_000002.12:29367043:C:T	(self)
ss17655009	NT_022184.13:8405842:C:T	NC_000002.12:29367043:C:T	(self)
ss44174771, ss66668980, ss66965463, ss67132410, ss70401735, ss70547103, ss71081071, ss75554409, ss85156650, ss121517312, ss153086175, ss159194669, ss160014835, ss161256147, ss169990159, ss171691190	NT_022184.15:8411796:C:T	NC_000002.12:29367043:C:T	(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 rs11893367

The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.

Genome context:

Select flank length:

Genomic regions, transcripts, and products
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NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

Choose placement

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs11893367