Name: rs1890395
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.

rs1890395

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr1:232396988 (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>A / T>C / T>G
Variation Type: SNV Single Nucleotide Variation
Frequency: C=0.267095 (82182/307688, ALFA)
C=0.305550 (80876/264690, TOPMED)
C=0.276458 (56695/205076, GENOGRAPHIC) (+ 22 more)
C=0.283083 (39635/140012, GnomAD)
C=0.38503 (30302/78700, PAGE_STUDY)
T=0.27959 (7900/28256, 14KJPN)
T=0.28144 (4717/16760, 8.3KJPN)
C=0.3913 (2506/6404, 1000G_30x)
C=0.4000 (2003/5008, 1000G)
C=0.2027 (908/4480, Estonian)
C=0.2608 (1005/3854, ALSPAC)
C=0.2754 (1021/3708, TWINSUK)
T=0.2700 (791/2930, KOREAN)
C=0.4175 (870/2084, HGDP_Stanford)
C=0.3732 (706/1892, HapMap)
T=0.2642 (484/1832, Korea1K)
C=0.253 (252/998, GoNL)
T=0.275 (217/788, PRJEB37584)
C=0.325 (195/600, NorthernSweden)
T=0.282 (98/348, SGDP_PRJ)
C=0.213 (46/216, Qatari)
T=0.319 (67/210, Vietnamese)
C=0.16 (10/64, Ancient Sardinia)
C=0.23 (9/40, GENOME_DK)
T=0.25 (6/24, Siberian)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: None
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	312818	T=0.732953	A=0.000000, C=0.267047
European	Sub	275896	T=0.747662	A=0.000000, C=0.252338
African	Sub	9296	T=0.7602	A=0.0000, C=0.2398
African Others	Sub	362	T=0.768	A=0.000, C=0.232
African American	Sub	8934	T=0.7599	A=0.0000, C=0.2401
Asian	Sub	3928	T=0.2925	A=0.0000, C=0.7075
East Asian	Sub	3184	T=0.2695	A=0.0000, C=0.7305
Other Asian	Sub	744	T=0.391	A=0.000, C=0.609
Latin American 1	Sub	1134	T=0.7196	A=0.0000, C=0.2804
Latin American 2	Sub	7212	T=0.4780	A=0.0000, C=0.5220
South Asian	Sub	5224	T=0.6776	A=0.0000, C=0.3224
Other	Sub	10128	T=0.68967	A=0.00000, C=0.31033

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	307688	T=0.732905	A=0.000000, C=0.267095
Allele Frequency Aggregator	European	Sub	272726	T=0.747633	A=0.000000, C=0.252367
Allele Frequency Aggregator	Other	Sub	9310	T=0.6940	A=0.0000, C=0.3060
Allele Frequency Aggregator	African	Sub	8154	T=0.7596	A=0.0000, C=0.2404
Allele Frequency Aggregator	Latin American 2	Sub	7212	T=0.4780	A=0.0000, C=0.5220
Allele Frequency Aggregator	South Asian	Sub	5224	T=0.6776	A=0.0000, C=0.3224
Allele Frequency Aggregator	Asian	Sub	3928	T=0.2925	A=0.0000, C=0.7075
Allele Frequency Aggregator	Latin American 1	Sub	1134	T=0.7196	A=0.0000, C=0.2804
TopMed	Global	Study-wide	264690	T=0.694450	C=0.305550
Genographic Project	Global	Study-wide	205076	T=0.723542	A=0.000000, C=0.276458
gnomAD - Genomes	Global	Study-wide	140012	T=0.716917	C=0.283083
gnomAD - Genomes	European	Sub	75848	T=0.73929	C=0.26071
gnomAD - Genomes	African	Sub	41938	T=0.75564	C=0.24436
gnomAD - Genomes	American	Sub	13622	T=0.56644	C=0.43356
gnomAD - Genomes	Ashkenazi Jewish	Sub	3320	T=0.7744	C=0.2256
gnomAD - Genomes	East Asian	Sub	3130	T=0.2681	C=0.7319
gnomAD - Genomes	Other	Sub	2154	T=0.6903	C=0.3097
The PAGE Study	Global	Study-wide	78700	T=0.61497	C=0.38503
The PAGE Study	AfricanAmerican	Sub	32514	T=0.74928	C=0.25072
The PAGE Study	Mexican	Sub	10810	T=0.47817	C=0.52183
The PAGE Study	Asian	Sub	8318	T=0.2715	C=0.7285
The PAGE Study	PuertoRican	Sub	7918	T=0.6519	C=0.3481
The PAGE Study	NativeHawaiian	Sub	4534	T=0.4446	C=0.5554
The PAGE Study	Cuban	Sub	4230	T=0.7184	C=0.2816
The PAGE Study	Dominican	Sub	3828	T=0.7202	C=0.2798
The PAGE Study	CentralAmerican	Sub	2450	T=0.5073	C=0.4927
The PAGE Study	SouthAmerican	Sub	1982	T=0.4909	C=0.5091
The PAGE Study	NativeAmerican	Sub	1260	T=0.6690	C=0.3310
The PAGE Study	SouthAsian	Sub	856	T=0.673	C=0.327
14KJPN	JAPANESE	Study-wide	28256	T=0.27959	C=0.72041
8.3KJPN	JAPANESE	Study-wide	16760	T=0.28144	C=0.71856
1000Genomes_30x	Global	Study-wide	6404	T=0.6087	C=0.3913
1000Genomes_30x	African	Sub	1786	T=0.7452	C=0.2548
1000Genomes_30x	Europe	Sub	1266	T=0.7496	C=0.2504
1000Genomes_30x	South Asian	Sub	1202	T=0.6622	C=0.3378
1000Genomes_30x	East Asian	Sub	1170	T=0.2632	C=0.7368
1000Genomes_30x	American	Sub	980	T=0.524	C=0.476
1000Genomes	Global	Study-wide	5008	T=0.6000	C=0.4000
1000Genomes	African	Sub	1322	T=0.7504	C=0.2496
1000Genomes	East Asian	Sub	1008	T=0.2629	C=0.7371
1000Genomes	Europe	Sub	1006	T=0.7346	C=0.2654
1000Genomes	South Asian	Sub	978	T=0.656	C=0.344
1000Genomes	American	Sub	694	T=0.529	C=0.471
Genetic variation in the Estonian population	Estonian	Study-wide	4480	T=0.7973	C=0.2027
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	T=0.7392	C=0.2608
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	T=0.7246	C=0.2754
KOREAN population from KRGDB	KOREAN	Study-wide	2930	T=0.2700	C=0.7300, G=0.0000
HGDP-CEPH-db Supplement 1	Global	Study-wide	2084	T=0.5825	C=0.4175
HGDP-CEPH-db Supplement 1	Est_Asia	Sub	470	T=0.272	C=0.728
HGDP-CEPH-db Supplement 1	Central_South_Asia	Sub	414	T=0.679	C=0.321
HGDP-CEPH-db Supplement 1	Middle_Est	Sub	350	T=0.774	C=0.226
HGDP-CEPH-db Supplement 1	Europe	Sub	320	T=0.762	C=0.237
HGDP-CEPH-db Supplement 1	Africa	Sub	242	T=0.748	C=0.252
HGDP-CEPH-db Supplement 1	America	Sub	216	T=0.287	C=0.713
HGDP-CEPH-db Supplement 1	Oceania	Sub	72	T=0.65	C=0.35
HapMap	Global	Study-wide	1892	T=0.6268	C=0.3732
HapMap	American	Sub	770	T=0.599	C=0.401
HapMap	African	Sub	692	T=0.789	C=0.211
HapMap	Asian	Sub	254	T=0.224	C=0.776
HapMap	Europe	Sub	176	T=0.693	C=0.307
Korean Genome Project	KOREAN	Study-wide	1832	T=0.2642	C=0.7358
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	T=0.747	C=0.253
CNV burdens in cranial meningiomas	Global	Study-wide	788	T=0.275	C=0.725
CNV burdens in cranial meningiomas	CRM	Sub	788	T=0.275	C=0.725
Northern Sweden	ACPOP	Study-wide	600	T=0.675	C=0.325
SGDP_PRJ	Global	Study-wide	348	T=0.282	C=0.718
Qatari	Global	Study-wide	216	T=0.787	C=0.213
A Vietnamese Genetic Variation Database	Global	Study-wide	210	T=0.319	C=0.681
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	64	T=0.84	C=0.16
The Danish reference pan genome	Danish	Study-wide	40	T=0.78	C=0.23
Siberian	Global	Study-wide	24	T=0.25	C=0.75

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.232396988T>A
GRCh38.p14 chr 1	NC_000001.11:g.232396988T>C
GRCh38.p14 chr 1	NC_000001.11:g.232396988T>G
GRCh37.p13 chr 1	NC_000001.10:g.232532734T>A
GRCh37.p13 chr 1	NC_000001.10:g.232532734T>C
GRCh37.p13 chr 1	NC_000001.10:g.232532734T>G

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=	A	C	G
GRCh38.p14 chr 1	NC_000001.11:g.232396988=	NC_000001.11:g.232396988T>A	NC_000001.11:g.232396988T>C	NC_000001.11:g.232396988T>G
GRCh37.p13 chr 1	NC_000001.10:g.232532734=	NC_000001.10:g.232532734T>A	NC_000001.10:g.232532734T>C	NC_000001.10:g.232532734T>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#.

129 SubSNP, 25 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	TSC-CSHL	ss2770997	Jan 12, 2001 (92)
2	BCM_SSAHASNP	ss9845646	Jul 11, 2003 (116)
3	ILLUMINA	ss66773368	Nov 30, 2006 (127)
4	ILLUMINA	ss67204068	Nov 30, 2006 (127)
5	ILLUMINA	ss67596304	Nov 30, 2006 (127)
6	ILLUMINA	ss70682294	May 25, 2008 (130)
7	ILLUMINA	ss71246147	May 17, 2007 (127)
8	ILLUMINA	ss75793809	Dec 07, 2007 (129)
9	ILLUMINA	ss79099311	Dec 15, 2007 (130)
10	KRIBB_YJKIM	ss83905658	Dec 15, 2007 (130)
11	BGI	ss102831758	Dec 01, 2009 (131)
12	1000GENOMES	ss109030857	Jan 23, 2009 (130)
13	ILLUMINA-UK	ss119245800	Feb 15, 2009 (130)
14	ILLUMINA	ss121840965	Dec 01, 2009 (131)
15	ILLUMINA	ss153767831	Dec 01, 2009 (131)
16	GMI	ss156415834	Dec 01, 2009 (131)
17	ILLUMINA	ss159337216	Dec 01, 2009 (131)
18	ILLUMINA	ss160473098	Dec 01, 2009 (131)
19	COMPLETE_GENOMICS	ss165895182	Jul 04, 2010 (132)
20	ILLUMINA	ss170865026	Jul 04, 2010 (132)
21	ILLUMINA	ss172969884	Jul 04, 2010 (132)
22	1000GENOMES	ss218940591	Jul 14, 2010 (132)
23	1000GENOMES	ss230945940	Jul 14, 2010 (132)
24	1000GENOMES	ss238551719	Jul 15, 2010 (132)
25	GMI	ss276261107	May 04, 2012 (137)
26	PJP	ss290755827	May 09, 2011 (134)
27	ILLUMINA	ss480332152	May 04, 2012 (137)
28	ILLUMINA	ss480343781	May 04, 2012 (137)
29	ILLUMINA	ss481107896	Sep 08, 2015 (146)
30	ILLUMINA	ss484963758	May 04, 2012 (137)
31	ILLUMINA	ss537004166	Sep 08, 2015 (146)
32	TISHKOFF	ss555208474	Apr 25, 2013 (138)
33	SSMP	ss648781550	Apr 25, 2013 (138)
34	ILLUMINA	ss778844886	Sep 08, 2015 (146)
35	ILLUMINA	ss782928185	Sep 08, 2015 (146)
36	ILLUMINA	ss783891040	Sep 08, 2015 (146)
37	ILLUMINA	ss825429829	Apr 01, 2015 (144)
38	ILLUMINA	ss832183517	Sep 08, 2015 (146)
39	ILLUMINA	ss832849195	Jul 12, 2019 (153)
40	ILLUMINA	ss834305475	Sep 08, 2015 (146)
41	EVA-GONL	ss976259503	Aug 21, 2014 (142)
42	JMKIDD_LAB	ss1068688358	Aug 21, 2014 (142)
43	1000GENOMES	ss1295083339	Aug 21, 2014 (142)
44	DDI	ss1426144558	Apr 01, 2015 (144)
45	EVA_GENOME_DK	ss1574751701	Apr 01, 2015 (144)
46	EVA_DECODE	ss1585659396	Apr 01, 2015 (144)
47	EVA_UK10K_ALSPAC	ss1602370621	Apr 01, 2015 (144)
48	EVA_UK10K_TWINSUK	ss1645364654	Apr 01, 2015 (144)
49	EVA_SVP	ss1712413990	Apr 01, 2015 (144)
50	ILLUMINA	ss1751905176	Sep 08, 2015 (146)
51	HAMMER_LAB	ss1795882743	Sep 08, 2015 (146)
52	WEILL_CORNELL_DGM	ss1919480837	Feb 12, 2016 (147)
53	ILLUMINA	ss1946026709	Feb 12, 2016 (147)
54	ILLUMINA	ss1958367352	Feb 12, 2016 (147)
55	GENOMED	ss1966999863	Jul 19, 2016 (147)
56	JJLAB	ss2020265707	Sep 14, 2016 (149)
57	USC_VALOUEV	ss2148301713	Dec 20, 2016 (150)
58	HUMAN_LONGEVITY	ss2170979166	Dec 20, 2016 (150)
59	SYSTEMSBIOZJU	ss2624645220	Nov 08, 2017 (151)
60	ILLUMINA	ss2632643501	Nov 08, 2017 (151)
61	ILLUMINA	ss2635008377	Nov 08, 2017 (151)
62	GRF	ss2698302595	Nov 08, 2017 (151)
63	ILLUMINA	ss2710697115	Nov 08, 2017 (151)
64	GNOMAD	ss2767444423	Nov 08, 2017 (151)
65	AFFY	ss2984897710	Nov 08, 2017 (151)
66	AFFY	ss2985541781	Nov 08, 2017 (151)
67	SWEGEN	ss2988628966	Nov 08, 2017 (151)
68	ILLUMINA	ss3021191445	Nov 08, 2017 (151)
69	BIOINF_KMB_FNS_UNIBA	ss3023893739	Nov 08, 2017 (151)
70	CSHL	ss3343962639	Nov 08, 2017 (151)
71	ILLUMINA	ss3625568890	Oct 11, 2018 (152)
72	ILLUMINA	ss3626333871	Oct 11, 2018 (152)
73	ILLUMINA	ss3630672616	Oct 11, 2018 (152)
74	ILLUMINA	ss3632929602	Oct 11, 2018 (152)
75	ILLUMINA	ss3633625860	Oct 11, 2018 (152)
76	ILLUMINA	ss3634378763	Oct 11, 2018 (152)
77	ILLUMINA	ss3635318862	Oct 11, 2018 (152)
78	ILLUMINA	ss3636057734	Oct 11, 2018 (152)
79	ILLUMINA	ss3637069415	Oct 11, 2018 (152)
80	ILLUMINA	ss3637820573	Oct 11, 2018 (152)
81	ILLUMINA	ss3638925315	Oct 11, 2018 (152)
82	ILLUMINA	ss3639461678	Oct 11, 2018 (152)
83	ILLUMINA	ss3640086116	Oct 11, 2018 (152)
84	ILLUMINA	ss3640993903	Oct 11, 2018 (152)
85	ILLUMINA	ss3641288046	Oct 11, 2018 (152)
86	ILLUMINA	ss3642826470	Oct 11, 2018 (152)
87	ILLUMINA	ss3644522715	Oct 11, 2018 (152)
88	ILLUMINA	ss3651537147	Oct 11, 2018 (152)
89	ILLUMINA	ss3653667874	Oct 11, 2018 (152)
90	EGCUT_WGS	ss3656587733	Jul 12, 2019 (153)
91	EVA_DECODE	ss3688843040	Jul 12, 2019 (153)
92	ILLUMINA	ss3725115658	Jul 12, 2019 (153)
93	ACPOP	ss3727956719	Jul 12, 2019 (153)
94	ILLUMINA	ss3744062451	Jul 12, 2019 (153)
95	ILLUMINA	ss3744679666	Jul 12, 2019 (153)
96	EVA	ss3747472877	Jul 12, 2019 (153)
97	PAGE_CC	ss3770879796	Jul 12, 2019 (153)
98	ILLUMINA	ss3772180465	Jul 12, 2019 (153)
99	KHV_HUMAN_GENOMES	ss3800474710	Jul 12, 2019 (153)
100	EVA	ss3826700416	Apr 25, 2020 (154)
101	EVA	ss3836751999	Apr 25, 2020 (154)
102	EVA	ss3842164503	Apr 25, 2020 (154)
103	HGDP	ss3847367040	Apr 25, 2020 (154)
104	SGDP_PRJ	ss3851123789	Apr 25, 2020 (154)
105	KRGDB	ss3896472602	Apr 25, 2020 (154)
106	KOGIC	ss3946718256	Apr 25, 2020 (154)
107	EVA	ss3984473893	Apr 25, 2021 (155)
108	EVA	ss3984859033	Apr 25, 2021 (155)
109	TOPMED	ss4487368110	Apr 25, 2021 (155)
110	TOMMO_GENOMICS	ss5148929571	Apr 25, 2021 (155)
111	1000G_HIGH_COVERAGE	ss5246174076	Oct 12, 2022 (156)
112	GENOGRAPHIC	ss5314472442	Oct 12, 2022 (156)
113	EVA	ss5314691077	Oct 12, 2022 (156)
114	EVA	ss5325481888	Oct 12, 2022 (156)
115	HUGCELL_USP	ss5446572016	Oct 12, 2022 (156)
116	EVA	ss5506228409	Oct 12, 2022 (156)
117	1000G_HIGH_COVERAGE	ss5520461256	Oct 12, 2022 (156)
118	SANFORD_IMAGENETICS	ss5624232979	Oct 12, 2022 (156)
119	SANFORD_IMAGENETICS	ss5627661965	Oct 12, 2022 (156)
120	TOMMO_GENOMICS	ss5676834213	Oct 12, 2022 (156)
121	EVA	ss5799515134	Oct 12, 2022 (156)
122	YY_MCH	ss5801735959	Oct 12, 2022 (156)
123	EVA	ss5833415615	Oct 12, 2022 (156)
124	EVA	ss5847176627	Oct 12, 2022 (156)
125	EVA	ss5847578378	Oct 12, 2022 (156)
126	EVA	ss5849333851	Oct 12, 2022 (156)
127	EVA	ss5912409560	Oct 12, 2022 (156)
128	EVA	ss5939510464	Oct 12, 2022 (156)
129	EVA	ss5979308664	Oct 12, 2022 (156)
130	1000Genomes	NC_000001.10 - 232532734	Oct 11, 2018 (152)
131	1000Genomes_30x	NC_000001.11 - 232396988	Oct 12, 2022 (156)
132	The Avon Longitudinal Study of Parents and Children	NC_000001.10 - 232532734	Oct 11, 2018 (152)
133	Genetic variation in the Estonian population	NC_000001.10 - 232532734	Oct 11, 2018 (152)
134	Genographic Project	NC_000001.11 - 232396988	Oct 12, 2022 (156)
135	The Danish reference pan genome	NC_000001.10 - 232532734	Apr 25, 2020 (154)
136	gnomAD - Genomes	NC_000001.11 - 232396988	Apr 25, 2021 (155)
137	Genome of the Netherlands Release 5	NC_000001.10 - 232532734	Apr 25, 2020 (154)
138	HGDP-CEPH-db Supplement 1	NC_000001.9 - 230599357	Apr 25, 2020 (154)
139	HapMap	NC_000001.11 - 232396988	Apr 25, 2020 (154)
140	KOREAN population from KRGDB	NC_000001.10 - 232532734	Apr 25, 2020 (154)
141	Korean Genome Project	NC_000001.11 - 232396988	Apr 25, 2020 (154)
142	Northern Sweden	NC_000001.10 - 232532734	Jul 12, 2019 (153)
143	The PAGE Study	NC_000001.11 - 232396988	Jul 12, 2019 (153)
144	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000001.10 - 232532734	Apr 25, 2021 (155)
145	CNV burdens in cranial meningiomas	NC_000001.10 - 232532734	Apr 25, 2021 (155)
146	Qatari	NC_000001.10 - 232532734	Apr 25, 2020 (154)
147	SGDP_PRJ	NC_000001.10 - 232532734	Apr 25, 2020 (154)
148	Siberian	NC_000001.10 - 232532734	Apr 25, 2020 (154)
149	8.3KJPN	NC_000001.10 - 232532734	Apr 25, 2021 (155)
150	14KJPN	NC_000001.11 - 232396988	Oct 12, 2022 (156)
151	TopMed	NC_000001.11 - 232396988	Apr 25, 2021 (155)
152	UK 10K study - Twins	NC_000001.10 - 232532734	Oct 11, 2018 (152)
153	A Vietnamese Genetic Variation Database	NC_000001.10 - 232532734	Jul 12, 2019 (153)
154	ALFA	NC_000001.11 - 232396988	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)
rs60202803	May 25, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
19229, 4509157860, ss5314472442	NC_000001.11:232396987:T:A	NC_000001.11:232396987:T:A	(self)
ss3638925315, ss3639461678	NC_000001.8:228839468:T:C	NC_000001.11:232396987:T:C	(self)
44932, ss109030857, ss119245800, ss165895182, ss276261107, ss290755827, ss480332152, ss825429829, ss1585659396, ss1712413990, ss2635008377, ss3642826470, ss3847367040	NC_000001.9:230599356:T:C	NC_000001.11:232396987:T:C	(self)
5953558, 3292494, 2325981, 1930491, 1439514, 3649996, 1241584, 84960, 23215, 1522767, 3140769, 818067, 6898878, 3292494, 716272, ss218940591, ss230945940, ss238551719, ss480343781, ss481107896, ss484963758, ss537004166, ss555208474, ss648781550, ss778844886, ss782928185, ss783891040, ss832183517, ss832849195, ss834305475, ss976259503, ss1068688358, ss1295083339, ss1426144558, ss1574751701, ss1602370621, ss1645364654, ss1751905176, ss1795882743, ss1919480837, ss1946026709, ss1958367352, ss1966999863, ss2020265707, ss2148301713, ss2624645220, ss2632643501, ss2698302595, ss2710697115, ss2767444423, ss2984897710, ss2985541781, ss2988628966, ss3021191445, ss3343962639, ss3625568890, ss3626333871, ss3630672616, ss3632929602, ss3633625860, ss3634378763, ss3635318862, ss3636057734, ss3637069415, ss3637820573, ss3640086116, ss3640993903, ss3641288046, ss3644522715, ss3651537147, ss3653667874, ss3656587733, ss3727956719, ss3744062451, ss3744679666, ss3747472877, ss3772180465, ss3826700416, ss3836751999, ss3851123789, ss3896472602, ss3984473893, ss3984859033, ss5148929571, ss5314691077, ss5325481888, ss5506228409, ss5624232979, ss5627661965, ss5799515134, ss5833415615, ss5847176627, ss5847578378, ss5939510464, ss5979308664	NC_000001.10:232532733:T:C	NC_000001.11:232396987:T:C	(self)
7987191, 19229, 42699270, 290772, 3096257, 101265, 10671317, 50974445, 4509157860, ss2170979166, ss3023893739, ss3688843040, ss3725115658, ss3770879796, ss3800474710, ss3842164503, ss3946718256, ss4487368110, ss5246174076, ss5314472442, ss5446572016, ss5520461256, ss5676834213, ss5801735959, ss5849333851, ss5912409560	NC_000001.11:232396987:T:C	NC_000001.11:232396987:T:C	(self)
ss9845646	NT_004433.15:171188:T:C	NC_000001.11:232396987:T:C	(self)
ss2770997, ss66773368, ss67204068, ss67596304, ss70682294, ss71246147, ss75793809, ss79099311, ss83905658, ss102831758, ss121840965, ss153767831, ss156415834, ss159337216, ss160473098, ss170865026, ss172969884	NT_167186.1:26050512:T:C	NC_000001.11:232396987:T:C	(self)
3649996, ss3896472602	NC_000001.10:232532733:T:G	NC_000001.11:232396987:T:G	(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 rs1890395

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

rs1890395