Name: rs2453274
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.

rs2453274

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr15:44482004 (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=0.046519 (12313/264690, TOPMED)
T=0.070857 (14467/204172, ALFA)
T=0.057019 (7995/140216, GnomAD) (+ 16 more)
T=0.0251 (161/6404, 1000G_30x)
T=0.0260 (130/5008, 1000G)
T=0.0882 (395/4480, Estonian)
T=0.0003 (1/2922, KOREAN)
T=0.0206 (43/2084, HGDP_Stanford)
T=0.0374 (42/1124, Daghestan)
T=0.065 (65/998, GoNL)
T=0.034 (33/982, HapMap)
T=0.004 (3/792, PRJEB37584)
T=0.122 (73/600, NorthernSweden)
T=0.028 (6/216, Qatari)
T=0.04 (2/56, Ancient Sardinia)
T=0.07 (3/40, GENOME_DK)
C=0.47 (14/30, SGDP_PRJ)
C=0.5 (3/6, Siberian)
T=0.5 (3/6, Siberian)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: CTDSPL2 : Intron Variant
Publications: 1 citation
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	204172	C=0.929143	T=0.070857
European	Sub	180782	C=0.924179	T=0.075821
African	Sub	7098	C=0.9846	T=0.0154
African Others	Sub	264	C=1.000	T=0.000
African American	Sub	6834	C=0.9841	T=0.0159
Asian	Sub	702	C=1.000	T=0.000
East Asian	Sub	556	C=1.000	T=0.000
Other Asian	Sub	146	C=1.000	T=0.000
Latin American 1	Sub	784	C=0.945	T=0.055
Latin American 2	Sub	2842	C=0.9662	T=0.0338
South Asian	Sub	5044	C=0.9782	T=0.0218
Other	Sub	6920	C=0.9419	T=0.0581

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=0.953481	T=0.046519
Allele Frequency Aggregator	Total	Global	204172	C=0.929143	T=0.070857
Allele Frequency Aggregator	European	Sub	180782	C=0.924179	T=0.075821
Allele Frequency Aggregator	African	Sub	7098	C=0.9846	T=0.0154
Allele Frequency Aggregator	Other	Sub	6920	C=0.9419	T=0.0581
Allele Frequency Aggregator	South Asian	Sub	5044	C=0.9782	T=0.0218
Allele Frequency Aggregator	Latin American 2	Sub	2842	C=0.9662	T=0.0338
Allele Frequency Aggregator	Latin American 1	Sub	784	C=0.945	T=0.055
Allele Frequency Aggregator	Asian	Sub	702	C=1.000	T=0.000
gnomAD - Genomes	Global	Study-wide	140216	C=0.942981	T=0.057019
gnomAD - Genomes	European	Sub	75910	C=0.91071	T=0.08929
gnomAD - Genomes	African	Sub	42040	C=0.98599	T=0.01401
gnomAD - Genomes	American	Sub	13656	C=0.96514	T=0.03486
gnomAD - Genomes	Ashkenazi Jewish	Sub	3324	C=0.9859	T=0.0141
gnomAD - Genomes	East Asian	Sub	3132	C=0.9997	T=0.0003
gnomAD - Genomes	Other	Sub	2154	C=0.9517	T=0.0483
1000Genomes_30x	Global	Study-wide	6404	C=0.9749	T=0.0251
1000Genomes_30x	African	Sub	1786	C=0.9983	T=0.0017
1000Genomes_30x	Europe	Sub	1266	C=0.9100	T=0.0900
1000Genomes_30x	South Asian	Sub	1202	C=0.9834	T=0.0166
1000Genomes_30x	East Asian	Sub	1170	C=1.0000	T=0.0000
1000Genomes_30x	American	Sub	980	C=0.976	T=0.024
1000Genomes	Global	Study-wide	5008	C=0.9740	T=0.0260
1000Genomes	African	Sub	1322	C=0.9977	T=0.0023
1000Genomes	East Asian	Sub	1008	C=1.0000	T=0.0000
1000Genomes	Europe	Sub	1006	C=0.9066	T=0.0934
1000Genomes	South Asian	Sub	978	C=0.985	T=0.015
1000Genomes	American	Sub	694	C=0.974	T=0.026
Genetic variation in the Estonian population	Estonian	Study-wide	4480	C=0.9118	T=0.0882
KOREAN population from KRGDB	KOREAN	Study-wide	2922	C=0.9997	T=0.0003
HGDP-CEPH-db Supplement 1	Global	Study-wide	2084	C=0.9794	T=0.0206
HGDP-CEPH-db Supplement 1	Est_Asia	Sub	470	C=0.998	T=0.002
HGDP-CEPH-db Supplement 1	Central_South_Asia	Sub	414	C=0.969	T=0.031
HGDP-CEPH-db Supplement 1	Middle_Est	Sub	350	C=0.977	T=0.023
HGDP-CEPH-db Supplement 1	Europe	Sub	320	C=0.941	T=0.059
HGDP-CEPH-db Supplement 1	Africa	Sub	242	C=1.000	T=0.000
HGDP-CEPH-db Supplement 1	America	Sub	216	C=0.991	T=0.009
HGDP-CEPH-db Supplement 1	Oceania	Sub	72	C=1.00	T=0.00
Genome-wide autozygosity in Daghestan	Global	Study-wide	1124	C=0.9626	T=0.0374
Genome-wide autozygosity in Daghestan	Daghestan	Sub	618	C=0.960	T=0.040
Genome-wide autozygosity in Daghestan	Near_East	Sub	142	C=0.965	T=0.035
Genome-wide autozygosity in Daghestan	Central Asia	Sub	122	C=0.967	T=0.033
Genome-wide autozygosity in Daghestan	Europe	Sub	108	C=0.944	T=0.056
Genome-wide autozygosity in Daghestan	South Asian	Sub	98	C=0.99	T=0.01
Genome-wide autozygosity in Daghestan	Caucasus	Sub	36	C=0.97	T=0.03
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	C=0.935	T=0.065
HapMap	Global	Study-wide	982	C=0.966	T=0.034
HapMap	American	Sub	600	C=0.968	T=0.032
HapMap	Europe	Sub	176	C=0.920	T=0.080
HapMap	African	Sub	118	C=1.000	T=0.000
HapMap	Asian	Sub	88	C=1.00	T=0.00
CNV burdens in cranial meningiomas	Global	Study-wide	792	C=0.996	T=0.004
CNV burdens in cranial meningiomas	CRM	Sub	792	C=0.996	T=0.004
Northern Sweden	ACPOP	Study-wide	600	C=0.878	T=0.122
Qatari	Global	Study-wide	216	C=0.972	T=0.028
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	56	C=0.96	T=0.04
The Danish reference pan genome	Danish	Study-wide	40	C=0.93	T=0.07
SGDP_PRJ	Global	Study-wide	30	C=0.47	T=0.53
Siberian	Global	Study-wide	6	C=0.5	T=0.5

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 15	NC_000015.10:g.44482004C>T
GRCh37.p13 chr 15	NC_000015.9:g.44774202C>T

Gene: CTDSPL2, CTD small phosphatase like 2 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
CTDSPL2 transcript	NM_016396.3:c.187-2220C>T	N/A	Intron Variant
CTDSPL2 transcript variant X2	XM_005254441.3:c.187-2220… XM_005254441.3:c.187-2220C>T	N/A	Intron Variant
CTDSPL2 transcript variant X1	XM_006720565.3:c.187-2220… XM_006720565.3:c.187-2220C>T	N/A	Intron Variant
CTDSPL2 transcript variant X3	XM_011521665.3:c.187-2220… XM_011521665.3:c.187-2220C>T	N/A	Intron Variant
CTDSPL2 transcript variant X4	XM_017022306.3:c.187-2220… XM_017022306.3:c.187-2220C>T	N/A	Intron Variant
CTDSPL2 transcript variant X10	XM_047432652.1:c.187-2220… XM_047432652.1:c.187-2220C>T	N/A	Intron Variant
CTDSPL2 transcript variant X11	XM_047432653.1:c.187-2220… XM_047432653.1:c.187-2220C>T	N/A	Intron Variant
CTDSPL2 transcript variant X12	XM_047432654.1:c.187-2220… XM_047432654.1:c.187-2220C>T	N/A	Intron Variant
CTDSPL2 transcript variant X13	XM_047432655.1:c.187-2220… XM_047432655.1:c.187-2220C>T	N/A	Intron Variant
CTDSPL2 transcript variant X5	XR_007064452.1:n.	N/A	Intron Variant
CTDSPL2 transcript variant X6	XR_007064453.1:n.	N/A	Intron Variant
CTDSPL2 transcript variant X7	XR_007064454.1:n.	N/A	Intron Variant
CTDSPL2 transcript variant X8	XR_007064455.1:n.	N/A	Intron Variant
CTDSPL2 transcript variant X9	XR_007064456.1: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	C=	T
GRCh38.p14 chr 15	NC_000015.10:g.44482004=	NC_000015.10:g.44482004C>T
GRCh37.p13 chr 15	NC_000015.9:g.44774202=	NC_000015.9:g.44774202C>T
CTDSPL2 transcript	NM_016396.2:c.187-2220=	NM_016396.2:c.187-2220C>T
CTDSPL2 transcript	NM_016396.3:c.187-2220=	NM_016396.3:c.187-2220C>T
CTDSPL2 transcript variant X1	XM_005254440.1:c.187-2220=	XM_005254440.1:c.187-2220C>T
CTDSPL2 transcript variant X2	XM_005254441.1:c.187-2220=	XM_005254441.1:c.187-2220C>T
CTDSPL2 transcript variant X2	XM_005254441.3:c.187-2220=	XM_005254441.3:c.187-2220C>T
CTDSPL2 transcript variant X1	XM_006720565.3:c.187-2220=	XM_006720565.3:c.187-2220C>T
CTDSPL2 transcript variant X3	XM_011521665.3:c.187-2220=	XM_011521665.3:c.187-2220C>T
CTDSPL2 transcript variant X4	XM_017022306.3:c.187-2220=	XM_017022306.3:c.187-2220C>T
CTDSPL2 transcript variant X10	XM_047432652.1:c.187-2220=	XM_047432652.1:c.187-2220C>T
CTDSPL2 transcript variant X11	XM_047432653.1:c.187-2220=	XM_047432653.1:c.187-2220C>T
CTDSPL2 transcript variant X12	XM_047432654.1:c.187-2220=	XM_047432654.1:c.187-2220C>T
CTDSPL2 transcript variant X13	XM_047432655.1:c.187-2220=	XM_047432655.1:c.187-2220C>T

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#.

83 SubSNP, 18 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	SC_JCM	ss3438727	Sep 28, 2001 (100)
2	ABI	ss43703771	Mar 14, 2006 (126)
3	ILLUMINA	ss67255332	Nov 30, 2006 (127)
4	ILLUMINA	ss67653601	Nov 30, 2006 (127)
5	ILLUMINA	ss68205363	Dec 12, 2006 (127)
6	ILLUMINA	ss70733681	May 23, 2008 (130)
7	ILLUMINA	ss71303522	May 17, 2007 (127)
8	ILLUMINA	ss75641773	Dec 06, 2007 (129)
9	KRIBB_YJKIM	ss84050601	Dec 14, 2007 (130)
10	1000GENOMES	ss108775658	Jan 23, 2009 (130)
11	ILLUMINA	ss153913465	Dec 01, 2009 (131)
12	ILLUMINA	ss159391253	Dec 01, 2009 (131)
13	ILLUMINA	ss160549230	Dec 01, 2009 (131)
14	ILLUMINA	ss173352855	Jul 04, 2010 (132)
15	1000GENOMES	ss236759859	Jul 15, 2010 (132)
16	ILLUMINA	ss480574333	May 04, 2012 (137)
17	ILLUMINA	ss480588817	May 04, 2012 (137)
18	ILLUMINA	ss481411240	Sep 08, 2015 (146)
19	ILLUMINA	ss485082687	May 04, 2012 (137)
20	ILLUMINA	ss537092820	Sep 08, 2015 (146)
21	ILLUMINA	ss778496777	Sep 08, 2015 (146)
22	ILLUMINA	ss782987646	Sep 08, 2015 (146)
23	ILLUMINA	ss783948516	Sep 08, 2015 (146)
24	ILLUMINA	ss832244366	Sep 08, 2015 (146)
25	ILLUMINA	ss832903002	Jul 13, 2019 (153)
26	ILLUMINA	ss833952838	Sep 08, 2015 (146)
27	EVA-GONL	ss991733510	Aug 21, 2014 (142)
28	1000GENOMES	ss1353256943	Aug 21, 2014 (142)
29	HAMMER_LAB	ss1397695690	Sep 08, 2015 (146)
30	EVA_GENOME_DK	ss1577585173	Apr 01, 2015 (144)
31	EVA_DECODE	ss1695748777	Apr 01, 2015 (144)
32	EVA_SVP	ss1713485871	Apr 01, 2015 (144)
33	ILLUMINA	ss1752160688	Sep 08, 2015 (146)
34	WEILL_CORNELL_DGM	ss1935137643	Feb 12, 2016 (147)
35	JJLAB	ss2028348319	Sep 14, 2016 (149)
36	USC_VALOUEV	ss2156747990	Dec 20, 2016 (150)
37	HUMAN_LONGEVITY	ss2206362792	Dec 20, 2016 (150)
38	ILLUMINA	ss2633222612	Nov 08, 2017 (151)
39	GNOMAD	ss2934305111	Nov 08, 2017 (151)
40	AFFY	ss2985040135	Nov 08, 2017 (151)
41	AFFY	ss2985672335	Nov 08, 2017 (151)
42	SWEGEN	ss3013198732	Nov 08, 2017 (151)
43	BIOINF_KMB_FNS_UNIBA	ss3027997486	Nov 08, 2017 (151)
44	CSHL	ss3351092169	Nov 08, 2017 (151)
45	ILLUMINA	ss3627349490	Oct 12, 2018 (152)
46	ILLUMINA	ss3631216049	Oct 12, 2018 (152)
47	ILLUMINA	ss3633095602	Oct 12, 2018 (152)
48	ILLUMINA	ss3633800154	Oct 12, 2018 (152)
49	ILLUMINA	ss3634604250	Oct 12, 2018 (152)
50	ILLUMINA	ss3635489108	Oct 12, 2018 (152)
51	ILLUMINA	ss3636294112	Oct 12, 2018 (152)
52	ILLUMINA	ss3637240368	Oct 12, 2018 (152)
53	ILLUMINA	ss3638082607	Oct 12, 2018 (152)
54	ILLUMINA	ss3639054481	Oct 12, 2018 (152)
55	ILLUMINA	ss3639836506	Oct 12, 2018 (152)
56	ILLUMINA	ss3640311573	Oct 12, 2018 (152)
57	ILLUMINA	ss3643066985	Oct 12, 2018 (152)
58	ILLUMINA	ss3643886674	Oct 12, 2018 (152)
59	ILLUMINA	ss3653811576	Oct 12, 2018 (152)
60	EGCUT_WGS	ss3680342544	Jul 13, 2019 (153)
61	EVA_DECODE	ss3697793485	Jul 13, 2019 (153)
62	ACPOP	ss3740879477	Jul 13, 2019 (153)
63	ILLUMINA	ss3744904795	Jul 13, 2019 (153)
64	EVA	ss3753020470	Jul 13, 2019 (153)
65	ILLUMINA	ss3772403458	Jul 13, 2019 (153)
66	EVA	ss3834208817	Apr 27, 2020 (154)
67	HGDP	ss3847521926	Apr 27, 2020 (154)
68	SGDP_PRJ	ss3882808888	Apr 27, 2020 (154)
69	KRGDB	ss3931960376	Apr 27, 2020 (154)
70	EVA	ss3984700489	Apr 27, 2021 (155)
71	EVA	ss3985713425	Apr 27, 2021 (155)
72	EVA	ss4017699113	Apr 27, 2021 (155)
73	TOPMED	ss4989533431	Apr 27, 2021 (155)
74	1000G_HIGH_COVERAGE	ss5298261688	Oct 16, 2022 (156)
75	EVA	ss5418906510	Oct 16, 2022 (156)
76	HUGCELL_USP	ss5492010117	Oct 16, 2022 (156)
77	1000G_HIGH_COVERAGE	ss5599572269	Oct 16, 2022 (156)
78	SANFORD_IMAGENETICS	ss5657406677	Oct 16, 2022 (156)
79	EVA	ss5799936372	Oct 16, 2022 (156)
80	EVA	ss5828133481	Oct 16, 2022 (156)
81	EVA	ss5875669998	Oct 16, 2022 (156)
82	EVA	ss5948804239	Oct 16, 2022 (156)
83	EVA	ss5980866428	Oct 16, 2022 (156)
84	1000Genomes	NC_000015.9 - 44774202	Oct 12, 2018 (152)
85	1000Genomes_30x	NC_000015.10 - 44482004	Oct 16, 2022 (156)
86	Genome-wide autozygosity in Daghestan	NC_000015.8 - 42561494	Apr 27, 2020 (154)
87	Genetic variation in the Estonian population	NC_000015.9 - 44774202	Oct 12, 2018 (152)
88	The Danish reference pan genome	NC_000015.9 - 44774202	Apr 27, 2020 (154)
89	gnomAD - Genomes	NC_000015.10 - 44482004	Apr 27, 2021 (155)
90	Genome of the Netherlands Release 5	NC_000015.9 - 44774202	Apr 27, 2020 (154)
91	HGDP-CEPH-db Supplement 1	NC_000015.8 - 42561494	Apr 27, 2020 (154)
92	HapMap	NC_000015.10 - 44482004	Apr 27, 2020 (154)
93	KOREAN population from KRGDB	NC_000015.9 - 44774202	Apr 27, 2020 (154)
94	Northern Sweden	NC_000015.9 - 44774202	Jul 13, 2019 (153)
95	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000015.9 - 44774202	Apr 27, 2021 (155)
96	CNV burdens in cranial meningiomas	NC_000015.9 - 44774202	Apr 27, 2021 (155)
97	Qatari	NC_000015.9 - 44774202	Apr 27, 2020 (154)
98	SGDP_PRJ	NC_000015.9 - 44774202	Apr 27, 2020 (154)
99	Siberian	NC_000015.9 - 44774202	Apr 27, 2020 (154)
100	TopMed	NC_000015.10 - 44482004	Apr 27, 2021 (155)
101	ALFA	NC_000015.10 - 44482004	Apr 27, 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)
rs57437027	May 23, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
165870, 199818, ss108775658, ss480574333, ss1397695690, ss1695748777, ss1713485871, ss3639054481, ss3639836506, ss3643066985, ss3643886674, ss3847521926	NC_000015.8:42561493:C:T	NC_000015.10:44482003:C:T	(self)
66321314, 26080792, 3835740, 16443258, 39137770, 14164342, 939352, 250011, 17179573, 34825868, 9264344, ss236759859, ss480588817, ss481411240, ss485082687, ss537092820, ss778496777, ss782987646, ss783948516, ss832244366, ss832903002, ss833952838, ss991733510, ss1353256943, ss1577585173, ss1752160688, ss1935137643, ss2028348319, ss2156747990, ss2633222612, ss2934305111, ss2985040135, ss2985672335, ss3013198732, ss3351092169, ss3627349490, ss3631216049, ss3633095602, ss3633800154, ss3634604250, ss3635489108, ss3636294112, ss3637240368, ss3638082607, ss3640311573, ss3653811576, ss3680342544, ss3740879477, ss3744904795, ss3753020470, ss3772403458, ss3834208817, ss3882808888, ss3931960376, ss3984700489, ss3985713425, ss4017699113, ss5418906510, ss5657406677, ss5799936372, ss5828133481, ss5948804239, ss5980866428	NC_000015.9:44774201:C:T	NC_000015.10:44482003:C:T	(self)
87098204, 467541726, 1252866, 205079091, 6729248671, ss2206362792, ss3027997486, ss3697793485, ss4989533431, ss5298261688, ss5492010117, ss5599572269, ss5875669998	NC_000015.10:44482003:C:T	NC_000015.10:44482003:C:T	(self)
ss3438727, ss43703771, ss67255332, ss67653601, ss68205363, ss70733681, ss71303522, ss75641773, ss84050601, ss153913465, ss159391253, ss160549230, ss173352855	NT_010194.17:15564758:C:T	NC_000015.10:44482003:C:T	(self)

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

1 citation for rs2453274

PMID	Title	Author	Year	Journal
22432041	Genome-wide association scan identifies a risk locus for preeclampsia on 2q14, near the inhibin, beta B gene.	Johnson MP et al.	2012	PloS one

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

rs2453274