Name: rs2357072
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.

rs2357072

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr1:232487859 (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>G / C>T
Variation Type: SNV Single Nucleotide Variation
Frequency: T=0.262534 (69490/264690, TOPMED)
T=0.252083 (35161/139482, GnomAD)
T=0.15653 (4423/28256, 14KJPN) (+ 17 more)
T=0.24506 (6173/25190, ALFA)
T=0.15811 (2650/16760, 8.3KJPN)
T=0.2511 (1608/6404, 1000G_30x)
T=0.2536 (1270/5008, 1000G)
T=0.2272 (1018/4480, Estonian)
T=0.2678 (1032/3854, ALSPAC)
T=0.2602 (965/3708, TWINSUK)
T=0.1874 (549/2930, KOREAN)
T=0.2217 (419/1890, HapMap)
T=0.272 (271/998, GoNL)
T=0.396 (248/626, Chileans)
T=0.288 (173/600, NorthernSweden)
C=0.396 (95/240, SGDP_PRJ)
T=0.167 (36/216, Qatari)
T=0.182 (39/214, Vietnamese)
T=0.30 (12/40, GENOME_DK)
C=0.47 (14/30, Siberian)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: SIPA1L2 : 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	25190	C=0.75494	G=0.00000, T=0.24506
European	Sub	17116	C=0.77647	G=0.00000, T=0.22353
African	Sub	3414	C=0.7786	G=0.0000, T=0.2214
African Others	Sub	114	C=0.772	G=0.000, T=0.228
African American	Sub	3300	C=0.7788	G=0.0000, T=0.2212
Asian	Sub	160	C=0.863	G=0.000, T=0.138
East Asian	Sub	102	C=0.853	G=0.000, T=0.147
Other Asian	Sub	58	C=0.88	G=0.00, T=0.12
Latin American 1	Sub	290	C=0.714	G=0.000, T=0.286
Latin American 2	Sub	2758	C=0.6222	G=0.0000, T=0.3778
South Asian	Sub	110	C=0.727	G=0.000, T=0.273
Other	Sub	1342	C=0.6915	G=0.0000, T=0.3085

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=0.737466	T=0.262534
gnomAD - Genomes	Global	Study-wide	139482	C=0.747917	T=0.252083
gnomAD - Genomes	European	Sub	75662	C=0.75808	T=0.24192
gnomAD - Genomes	African	Sub	41660	C=0.74592	T=0.25408
gnomAD - Genomes	American	Sub	13590	C=0.65578	T=0.34422
gnomAD - Genomes	Ashkenazi Jewish	Sub	3314	C=0.8395	T=0.1605
gnomAD - Genomes	East Asian	Sub	3114	C=0.8398	T=0.1602
gnomAD - Genomes	Other	Sub	2142	C=0.7372	T=0.2628
14KJPN	JAPANESE	Study-wide	28256	C=0.84347	T=0.15653
Allele Frequency Aggregator	Total	Global	25190	C=0.75494	G=0.00000, T=0.24506
Allele Frequency Aggregator	European	Sub	17116	C=0.77647	G=0.00000, T=0.22353
Allele Frequency Aggregator	African	Sub	3414	C=0.7786	G=0.0000, T=0.2214
Allele Frequency Aggregator	Latin American 2	Sub	2758	C=0.6222	G=0.0000, T=0.3778
Allele Frequency Aggregator	Other	Sub	1342	C=0.6915	G=0.0000, T=0.3085
Allele Frequency Aggregator	Latin American 1	Sub	290	C=0.714	G=0.000, T=0.286
Allele Frequency Aggregator	Asian	Sub	160	C=0.863	G=0.000, T=0.138
Allele Frequency Aggregator	South Asian	Sub	110	C=0.727	G=0.000, T=0.273
8.3KJPN	JAPANESE	Study-wide	16760	C=0.84189	T=0.15811
1000Genomes_30x	Global	Study-wide	6404	C=0.7489	T=0.2511
1000Genomes_30x	African	Sub	1786	C=0.7794	T=0.2206
1000Genomes_30x	Europe	Sub	1266	C=0.7662	T=0.2338
1000Genomes_30x	South Asian	Sub	1202	C=0.7047	T=0.2953
1000Genomes_30x	East Asian	Sub	1170	C=0.8410	T=0.1590
1000Genomes_30x	American	Sub	980	C=0.615	T=0.385
1000Genomes	Global	Study-wide	5008	C=0.7464	T=0.2536
1000Genomes	African	Sub	1322	C=0.7700	T=0.2300
1000Genomes	East Asian	Sub	1008	C=0.8353	T=0.1647
1000Genomes	Europe	Sub	1006	C=0.7674	T=0.2326
1000Genomes	South Asian	Sub	978	C=0.700	T=0.300
1000Genomes	American	Sub	694	C=0.607	T=0.393
Genetic variation in the Estonian population	Estonian	Study-wide	4480	C=0.7728	T=0.2272
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	C=0.7322	T=0.2678
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	C=0.7398	T=0.2602
KOREAN population from KRGDB	KOREAN	Study-wide	2930	C=0.8126	T=0.1874
HapMap	Global	Study-wide	1890	C=0.7783	T=0.2217
HapMap	American	Sub	768	C=0.770	T=0.230
HapMap	African	Sub	692	C=0.753	T=0.247
HapMap	Asian	Sub	254	C=0.843	T=0.157
HapMap	Europe	Sub	176	C=0.824	T=0.176
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	C=0.728	T=0.272
Chileans	Chilean	Study-wide	626	C=0.604	T=0.396
Northern Sweden	ACPOP	Study-wide	600	C=0.712	T=0.288
SGDP_PRJ	Global	Study-wide	240	C=0.396	T=0.604
Qatari	Global	Study-wide	216	C=0.833	T=0.167
A Vietnamese Genetic Variation Database	Global	Study-wide	214	C=0.818	T=0.182
The Danish reference pan genome	Danish	Study-wide	40	C=0.70	T=0.30
Siberian	Global	Study-wide	30	C=0.47	T=0.53

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.232487859C>G
GRCh38.p14 chr 1	NC_000001.11:g.232487859C>T
GRCh37.p13 chr 1	NC_000001.10:g.232623605C>G
GRCh37.p13 chr 1	NC_000001.10:g.232623605C>T

Gene: SIPA1L2, signal induced proliferation associated 1 like 2 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
SIPA1L2 transcript variant 2	NM_001377488.1:c.1806+301… NM_001377488.1:c.1806+3015G>C	N/A	Intron Variant
SIPA1L2 transcript variant 1	NM_020808.5:c.1806+3015G>C	N/A	Intron Variant
SIPA1L2 transcript variant X8	XM_005273213.5:c.1806+301… XM_005273213.5:c.1806+3015G>C	N/A	Intron Variant
SIPA1L2 transcript variant X5	XM_017001896.2:c.1806+301… XM_017001896.2:c.1806+3015G>C	N/A	Intron Variant
SIPA1L2 transcript variant X1	XM_047426139.1:c.1806+301… XM_047426139.1:c.1806+3015G>C	N/A	Intron Variant
SIPA1L2 transcript variant X2	XM_047426140.1:c.1806+301… XM_047426140.1:c.1806+3015G>C	N/A	Intron Variant
SIPA1L2 transcript variant X3	XM_047426141.1:c.1806+301… XM_047426141.1:c.1806+3015G>C	N/A	Intron Variant
SIPA1L2 transcript variant X4	XM_047426142.1:c.1806+301… XM_047426142.1:c.1806+3015G>C	N/A	Intron Variant
SIPA1L2 transcript variant X6	XM_047426143.1:c.1806+301… XM_047426143.1:c.1806+3015G>C	N/A	Intron Variant
SIPA1L2 transcript variant X7	XM_047426144.1:c.1806+301… XM_047426144.1:c.1806+3015G>C	N/A	Intron Variant
SIPA1L2 transcript variant X9	XM_047426145.1:c.1806+301… XM_047426145.1:c.1806+3015G>C	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=	G	T
GRCh38.p14 chr 1	NC_000001.11:g.232487859=	NC_000001.11:g.232487859C>G	NC_000001.11:g.232487859C>T
GRCh37.p13 chr 1	NC_000001.10:g.232623605=	NC_000001.10:g.232623605C>G	NC_000001.10:g.232623605C>T
SIPA1L2 transcript variant 2	NM_001377488.1:c.1806+3015=	NM_001377488.1:c.1806+3015G>C	NM_001377488.1:c.1806+3015G>A
SIPA1L2 transcript	NM_020808.3:c.1806+3015=	NM_020808.3:c.1806+3015G>C	NM_020808.3:c.1806+3015G>A
SIPA1L2 transcript variant 1	NM_020808.5:c.1806+3015=	NM_020808.5:c.1806+3015G>C	NM_020808.5:c.1806+3015G>A
SIPA1L2 transcript variant X1	XM_005273209.1:c.1806+3015=	XM_005273209.1:c.1806+3015G>C	XM_005273209.1:c.1806+3015G>A
SIPA1L2 transcript variant X2	XM_005273210.1:c.1806+3015=	XM_005273210.1:c.1806+3015G>C	XM_005273210.1:c.1806+3015G>A
SIPA1L2 transcript variant X4	XM_005273211.1:c.1806+3015=	XM_005273211.1:c.1806+3015G>C	XM_005273211.1:c.1806+3015G>A
SIPA1L2 transcript variant X4	XM_005273212.1:c.1806+3015=	XM_005273212.1:c.1806+3015G>C	XM_005273212.1:c.1806+3015G>A
SIPA1L2 transcript variant X5	XM_005273213.1:c.1806+3015=	XM_005273213.1:c.1806+3015G>C	XM_005273213.1:c.1806+3015G>A
SIPA1L2 transcript variant X8	XM_005273213.5:c.1806+3015=	XM_005273213.5:c.1806+3015G>C	XM_005273213.5:c.1806+3015G>A
SIPA1L2 transcript variant X8	XM_005273214.1:c.1806+3015=	XM_005273214.1:c.1806+3015G>C	XM_005273214.1:c.1806+3015G>A
SIPA1L2 transcript variant X7	XM_005273215.1:c.1806+3015=	XM_005273215.1:c.1806+3015G>C	XM_005273215.1:c.1806+3015G>A
SIPA1L2 transcript variant X5	XM_017001896.2:c.1806+3015=	XM_017001896.2:c.1806+3015G>C	XM_017001896.2:c.1806+3015G>A
SIPA1L2 transcript variant X1	XM_047426139.1:c.1806+3015=	XM_047426139.1:c.1806+3015G>C	XM_047426139.1:c.1806+3015G>A
SIPA1L2 transcript variant X2	XM_047426140.1:c.1806+3015=	XM_047426140.1:c.1806+3015G>C	XM_047426140.1:c.1806+3015G>A
SIPA1L2 transcript variant X3	XM_047426141.1:c.1806+3015=	XM_047426141.1:c.1806+3015G>C	XM_047426141.1:c.1806+3015G>A
SIPA1L2 transcript variant X4	XM_047426142.1:c.1806+3015=	XM_047426142.1:c.1806+3015G>C	XM_047426142.1:c.1806+3015G>A
SIPA1L2 transcript variant X6	XM_047426143.1:c.1806+3015=	XM_047426143.1:c.1806+3015G>C	XM_047426143.1:c.1806+3015G>A
SIPA1L2 transcript variant X7	XM_047426144.1:c.1806+3015=	XM_047426144.1:c.1806+3015G>C	XM_047426144.1:c.1806+3015G>A
SIPA1L2 transcript variant X9	XM_047426145.1:c.1806+3015=	XM_047426145.1:c.1806+3015G>C	XM_047426145.1:c.1806+3015G>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#.

70 SubSNP, 20 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	TSC-CSHL	ss3313072	Sep 28, 2001 (100)
2	CSHL-HAPMAP	ss19114109	Feb 27, 2004 (120)
3	SSAHASNP	ss20477412	Apr 05, 2004 (121)
4	PERLEGEN	ss23894507	Sep 20, 2004 (123)
5	ABI	ss44120139	Mar 15, 2006 (126)
6	AFFY	ss66184193	Nov 30, 2006 (127)
7	AFFY	ss76252580	Dec 06, 2007 (129)
8	KRIBB_YJKIM	ss81771025	Dec 15, 2007 (130)
9	HUMANGENOME_JCVI	ss98011096	Feb 06, 2009 (130)
10	BGI	ss102831877	Dec 01, 2009 (131)
11	1000GENOMES	ss109031562	Jan 23, 2009 (130)
12	1000GENOMES	ss111934609	Jan 25, 2009 (130)
13	ENSEMBL	ss139036782	Dec 01, 2009 (131)
14	COMPLETE_GENOMICS	ss165399372	Jul 04, 2010 (132)
15	AFFY	ss172983814	Jul 04, 2010 (132)
16	BUSHMAN	ss199747297	Jul 04, 2010 (132)
17	BCM-HGSC-SUB	ss205055027	Jul 04, 2010 (132)
18	1000GENOMES	ss218940991	Jul 14, 2010 (132)
19	1000GENOMES	ss230946200	Jul 14, 2010 (132)
20	1000GENOMES	ss238551985	Jul 15, 2010 (132)
21	GMI	ss276261433	May 04, 2012 (137)
22	GMI	ss284247514	Apr 25, 2013 (138)
23	PJP	ss290756004	May 09, 2011 (134)
24	TISHKOFF	ss555208871	Apr 25, 2013 (138)
25	SSMP	ss648781998	Apr 25, 2013 (138)
26	EVA-GONL	ss976260245	Aug 21, 2014 (142)
27	JMKIDD_LAB	ss1068688893	Aug 21, 2014 (142)
28	1000GENOMES	ss1295086036	Aug 21, 2014 (142)
29	EVA_GENOME_DK	ss1574752244	Apr 01, 2015 (144)
30	EVA_DECODE	ss1585660123	Apr 01, 2015 (144)
31	EVA_UK10K_ALSPAC	ss1602372142	Apr 01, 2015 (144)
32	EVA_UK10K_TWINSUK	ss1645366175	Apr 01, 2015 (144)
33	EVA_SVP	ss1712414103	Apr 01, 2015 (144)
34	HAMMER_LAB	ss1795883502	Sep 08, 2015 (146)
35	WEILL_CORNELL_DGM	ss1919481465	Feb 12, 2016 (147)
36	GENOMED	ss1967000105	Jul 19, 2016 (147)
37	JJLAB	ss2020266066	Sep 14, 2016 (149)
38	USC_VALOUEV	ss2148302092	Dec 20, 2016 (150)
39	HUMAN_LONGEVITY	ss2170984738	Dec 20, 2016 (150)
40	GRF	ss2698303007	Nov 08, 2017 (151)
41	GNOMAD	ss2767451515	Nov 08, 2017 (151)
42	SWEGEN	ss2988629960	Nov 08, 2017 (151)
43	BIOINF_KMB_FNS_UNIBA	ss3023893924	Nov 08, 2017 (151)
44	CSHL	ss3343962947	Nov 08, 2017 (151)
45	URBANLAB	ss3646910629	Oct 11, 2018 (152)
46	EGCUT_WGS	ss3656588877	Jul 12, 2019 (153)
47	EVA_DECODE	ss3688844197	Jul 12, 2019 (153)
48	ACPOP	ss3727957301	Jul 12, 2019 (153)
49	EVA	ss3747473744	Jul 12, 2019 (153)
50	KHV_HUMAN_GENOMES	ss3800475519	Jul 12, 2019 (153)
51	EVA	ss3826700760	Apr 25, 2020 (154)
52	EVA	ss3836752188	Apr 25, 2020 (154)
53	EVA	ss3842164695	Apr 25, 2020 (154)
54	SGDP_PRJ	ss3851124981	Apr 25, 2020 (154)
55	KRGDB	ss3896473996	Apr 25, 2020 (154)
56	TOPMED	ss4487391253	Apr 25, 2021 (155)
57	TOMMO_GENOMICS	ss5148932322	Apr 25, 2021 (155)
58	1000G_HIGH_COVERAGE	ss5246176251	Oct 12, 2022 (156)
59	EVA	ss5325486261	Oct 12, 2022 (156)
60	HUGCELL_USP	ss5446574038	Oct 12, 2022 (156)
61	EVA	ss5506228617	Oct 12, 2022 (156)
62	1000G_HIGH_COVERAGE	ss5520464641	Oct 12, 2022 (156)
63	SANFORD_IMAGENETICS	ss5627663288	Oct 12, 2022 (156)
64	TOMMO_GENOMICS	ss5676837734	Oct 12, 2022 (156)
65	YY_MCH	ss5801736519	Oct 12, 2022 (156)
66	EVA	ss5833416549	Oct 12, 2022 (156)
67	EVA	ss5849334168	Oct 12, 2022 (156)
68	EVA	ss5912412349	Oct 12, 2022 (156)
69	EVA	ss5939511873	Oct 12, 2022 (156)
70	EVA	ss5980022061	Oct 12, 2022 (156)
71	1000Genomes	NC_000001.10 - 232623605	Oct 11, 2018 (152)
72	1000Genomes_30x	NC_000001.11 - 232487859	Oct 12, 2022 (156)
73	The Avon Longitudinal Study of Parents and Children	NC_000001.10 - 232623605	Oct 11, 2018 (152)
74	Chileans	NC_000001.10 - 232623605	Apr 25, 2020 (154)
75	Genetic variation in the Estonian population	NC_000001.10 - 232623605	Oct 11, 2018 (152)
76	The Danish reference pan genome	NC_000001.10 - 232623605	Apr 25, 2020 (154)
77	gnomAD - Genomes	NC_000001.11 - 232487859	Apr 25, 2021 (155)
78	Genome of the Netherlands Release 5	NC_000001.10 - 232623605	Apr 25, 2020 (154)
79	HapMap	NC_000001.11 - 232487859	Apr 25, 2020 (154)
80	KOREAN population from KRGDB	NC_000001.10 - 232623605	Apr 25, 2020 (154)
81	Northern Sweden	NC_000001.10 - 232623605	Jul 12, 2019 (153)
82	Qatari	NC_000001.10 - 232623605	Apr 25, 2020 (154)
83	SGDP_PRJ	NC_000001.10 - 232623605	Apr 25, 2020 (154)
84	Siberian	NC_000001.10 - 232623605	Apr 25, 2020 (154)
85	8.3KJPN	NC_000001.10 - 232623605	Apr 25, 2021 (155)
86	14KJPN	NC_000001.11 - 232487859	Oct 12, 2022 (156)
87	TopMed	NC_000001.11 - 232487859	Apr 25, 2021 (155)
88	UK 10K study - Twins	NC_000001.10 - 232623605	Oct 11, 2018 (152)
89	A Vietnamese Genetic Variation Database	NC_000001.10 - 232623605	Jul 12, 2019 (153)
90	ALFA	NC_000001.11 - 232487859	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)
rs60645457	Feb 27, 2009 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
7856221827	NC_000001.11:232487858:C:G	NC_000001.11:232487858:C:G	(self)
ss66184193, ss76252580, ss109031562, ss111934609, ss165399372, ss172983814, ss199747297, ss205055027, ss276261433, ss284247514, ss290756004, ss1585660123, ss1712414103	NC_000001.9:230690227:C:T	NC_000001.11:232487858:C:T	(self)
5956345, 3294132, 36064, 2327125, 1930770, 1440256, 3651390, 1242166, 1523395, 3141961, 818446, 6901629, 3294132, 716664, ss218940991, ss230946200, ss238551985, ss555208871, ss648781998, ss976260245, ss1068688893, ss1295086036, ss1574752244, ss1602372142, ss1645366175, ss1795883502, ss1919481465, ss1967000105, ss2020266066, ss2148302092, ss2698303007, ss2767451515, ss2988629960, ss3343962947, ss3656588877, ss3727957301, ss3747473744, ss3826700760, ss3836752188, ss3851124981, ss3896473996, ss5148932322, ss5325486261, ss5506228617, ss5627663288, ss5833416549, ss5939511873, ss5980022061	NC_000001.10:232623604:C:T	NC_000001.11:232487858:C:T	(self)
7990576, 42717549, 291021, 10674838, 50997588, 7856221827, ss2170984738, ss3023893924, ss3646910629, ss3688844197, ss3800475519, ss3842164695, ss4487391253, ss5246176251, ss5446574038, ss5520464641, ss5676837734, ss5801736519, ss5849334168, ss5912412349	NC_000001.11:232487858:C:T	NC_000001.11:232487858:C:T	(self)
ss19114109, ss20477412	NT_004433.16:298953:C:T	NC_000001.11:232487858:C:T	(self)
ss3313072, ss23894507, ss44120139, ss81771025, ss98011096, ss102831877, ss139036782	NT_167186.1:26141383:C:T	NC_000001.11:232487858: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 rs2357072

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

rs2357072