Name: rs273882
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.

rs273882

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr1:96811132 (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
Variation Type: SNV Single Nucleotide Variation
Frequency: C=0.294813 (78034/264690, TOPMED)
C=0.283999 (39711/139828, GnomAD)
C=0.42710 (12068/28256, 14KJPN) (+ 17 more)
C=0.30330 (7486/24682, ALFA)
C=0.42601 (7140/16760, 8.3KJPN)
C=0.3364 (2154/6404, 1000G_30x)
C=0.3431 (1718/5008, 1000G)
C=0.2703 (1211/4480, Estonian)
C=0.3373 (1300/3854, ALSPAC)
C=0.3417 (1267/3708, TWINSUK)
C=0.4249 (1245/2930, KOREAN)
C=0.4269 (782/1832, Korea1K)
C=0.314 (313/998, GoNL)
C=0.310 (186/600, NorthernSweden)
T=0.332 (113/340, SGDP_PRJ)
C=0.255 (81/318, HapMap)
C=0.185 (40/216, Qatari)
C=0.495 (103/208, Vietnamese)
C=0.38 (15/40, GENOME_DK)
T=0.42 (10/24, Siberian)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: PTBP2 : 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	24776	T=0.69644	A=0.00000, C=0.30356
European	Sub	20066	T=0.67507	A=0.00000, C=0.32493
African	Sub	2790	T=0.8717	A=0.0000, C=0.1283
African Others	Sub	102	T=0.941	A=0.000, C=0.059
African American	Sub	2688	T=0.8690	A=0.0000, C=0.1310
Asian	Sub	112	T=0.527	A=0.000, C=0.473
East Asian	Sub	86	T=0.53	A=0.00, C=0.47
Other Asian	Sub	26	T=0.50	A=0.00, C=0.50
Latin American 1	Sub	146	T=0.753	A=0.000, C=0.247
Latin American 2	Sub	610	T=0.664	A=0.000, C=0.336
South Asian	Sub	98	T=0.61	A=0.00, C=0.39
Other	Sub	954	T=0.674	A=0.000, C=0.326

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	T=0.705187	C=0.294813
gnomAD - Genomes	Global	Study-wide	139828	T=0.716001	C=0.283999
gnomAD - Genomes	European	Sub	75696	T=0.67455	C=0.32545
gnomAD - Genomes	African	Sub	41916	T=0.84051	C=0.15949
gnomAD - Genomes	American	Sub	13634	T=0.64053	C=0.35947
gnomAD - Genomes	Ashkenazi Jewish	Sub	3324	T=0.6143	C=0.3857
gnomAD - Genomes	East Asian	Sub	3122	T=0.5237	C=0.4763
gnomAD - Genomes	Other	Sub	2136	T=0.6625	C=0.3375
14KJPN	JAPANESE	Study-wide	28256	T=0.57290	C=0.42710
Allele Frequency Aggregator	Total	Global	24682	T=0.69670	A=0.00000, C=0.30330
Allele Frequency Aggregator	European	Sub	19990	T=0.67534	A=0.00000, C=0.32466
Allele Frequency Aggregator	African	Sub	2790	T=0.8717	A=0.0000, C=0.1283
Allele Frequency Aggregator	Other	Sub	936	T=0.673	A=0.000, C=0.327
Allele Frequency Aggregator	Latin American 2	Sub	610	T=0.664	A=0.000, C=0.336
Allele Frequency Aggregator	Latin American 1	Sub	146	T=0.753	A=0.000, C=0.247
Allele Frequency Aggregator	Asian	Sub	112	T=0.527	A=0.000, C=0.473
Allele Frequency Aggregator	South Asian	Sub	98	T=0.61	A=0.00, C=0.39
8.3KJPN	JAPANESE	Study-wide	16760	T=0.57399	C=0.42601
1000Genomes_30x	Global	Study-wide	6404	T=0.6636	C=0.3364
1000Genomes_30x	African	Sub	1786	T=0.8813	C=0.1187
1000Genomes_30x	Europe	Sub	1266	T=0.6698	C=0.3302
1000Genomes_30x	South Asian	Sub	1202	T=0.5075	C=0.4925
1000Genomes_30x	East Asian	Sub	1170	T=0.5376	C=0.4624
1000Genomes_30x	American	Sub	980	T=0.601	C=0.399
1000Genomes	Global	Study-wide	5008	T=0.6569	C=0.3431
1000Genomes	African	Sub	1322	T=0.8782	C=0.1218
1000Genomes	East Asian	Sub	1008	T=0.5427	C=0.4573
1000Genomes	Europe	Sub	1006	T=0.6690	C=0.3310
1000Genomes	South Asian	Sub	978	T=0.503	C=0.497
1000Genomes	American	Sub	694	T=0.601	C=0.399
Genetic variation in the Estonian population	Estonian	Study-wide	4480	T=0.7297	C=0.2703
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	T=0.6627	C=0.3373
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	T=0.6583	C=0.3417
KOREAN population from KRGDB	KOREAN	Study-wide	2930	T=0.5751	A=0.0000, C=0.4249
Korean Genome Project	KOREAN	Study-wide	1832	T=0.5731	C=0.4269
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	T=0.686	C=0.314
Northern Sweden	ACPOP	Study-wide	600	T=0.690	C=0.310
SGDP_PRJ	Global	Study-wide	340	T=0.332	C=0.668
HapMap	Global	Study-wide	318	T=0.745	C=0.255
HapMap	African	Sub	116	T=0.940	C=0.060
HapMap	American	Sub	114	T=0.684	C=0.316
HapMap	Asian	Sub	88	T=0.57	C=0.43
Qatari	Global	Study-wide	216	T=0.815	C=0.185
A Vietnamese Genetic Variation Database	Global	Study-wide	208	T=0.505	C=0.495
The Danish reference pan genome	Danish	Study-wide	40	T=0.62	C=0.38
Siberian	Global	Study-wide	24	T=0.42	C=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 1	NC_000001.11:g.96811132T>A
GRCh38.p14 chr 1	NC_000001.11:g.96811132T>C
GRCh37.p13 chr 1	NC_000001.10:g.97276688T>A
GRCh37.p13 chr 1	NC_000001.10:g.97276688T>C

Gene: PTBP2, polypyrimidine tract binding protein 2 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
PTBP2 transcript variant 1	NM_001300985.2:c.1187-158… NM_001300985.2:c.1187-1580T>A	N/A	Intron Variant
PTBP2 transcript variant 2	NM_001300986.2:c.1196-158… NM_001300986.2:c.1196-1580T>A	N/A	Intron Variant
PTBP2 transcript variant 3	NM_001300987.2:c.1220-158… NM_001300987.2:c.1220-1580T>A	N/A	Intron Variant
PTBP2 transcript variant 4	NM_001300988.2:c.1187-158… NM_001300988.2:c.1187-1580T>A	N/A	Intron Variant
PTBP2 transcript variant 5	NM_001300989.2:c.1172-158… NM_001300989.2:c.1172-1580T>A	N/A	Intron Variant
PTBP2 transcript variant 7	NM_001300990.2:c.1016-158… NM_001300990.2:c.1016-1580T>A	N/A	Intron Variant
PTBP2 transcript variant 6	NM_021190.4:c.1172-1580T>A	N/A	Intron Variant
PTBP2 transcript variant 9	NR_125356.1:n.	N/A	Intron Variant
PTBP2 transcript variant 8	NR_125357.2:n.	N/A	Intron Variant
PTBP2 transcript variant X2	XM_011541874.3:c.1211-158… XM_011541874.3:c.1211-1580T>A	N/A	Intron Variant
PTBP2 transcript variant X3	XM_011541875.3:c.1196-158… XM_011541875.3:c.1196-1580T>A	N/A	Intron Variant
PTBP2 transcript variant X1	XM_011541876.3:c.1211-158… XM_011541876.3:c.1211-1580T>A	N/A	Intron Variant
PTBP2 transcript variant X6	XM_017001951.2:c.1220-158… XM_017001951.2:c.1220-1580T>A	N/A	Intron Variant
PTBP2 transcript variant X3	XM_047426537.1:c.1094-158… XM_047426537.1:c.1094-1580T>A	N/A	Intron Variant
PTBP2 transcript variant X4	XM_047426538.1:c.	N/A	Genic Downstream Transcript Variant
PTBP2 transcript variant X5	XM_047426539.1:c.	N/A	Genic Downstream Transcript 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=	A	C
GRCh38.p14 chr 1	NC_000001.11:g.96811132=	NC_000001.11:g.96811132T>A	NC_000001.11:g.96811132T>C
GRCh37.p13 chr 1	NC_000001.10:g.97276688=	NC_000001.10:g.97276688T>A	NC_000001.10:g.97276688T>C
PTBP2 transcript variant 1	NM_001300985.2:c.1187-1580=	NM_001300985.2:c.1187-1580T>A	NM_001300985.2:c.1187-1580T>C
PTBP2 transcript variant 2	NM_001300986.2:c.1196-1580=	NM_001300986.2:c.1196-1580T>A	NM_001300986.2:c.1196-1580T>C
PTBP2 transcript variant 3	NM_001300987.2:c.1220-1580=	NM_001300987.2:c.1220-1580T>A	NM_001300987.2:c.1220-1580T>C
PTBP2 transcript variant 4	NM_001300988.2:c.1187-1580=	NM_001300988.2:c.1187-1580T>A	NM_001300988.2:c.1187-1580T>C
PTBP2 transcript variant 5	NM_001300989.2:c.1172-1580=	NM_001300989.2:c.1172-1580T>A	NM_001300989.2:c.1172-1580T>C
PTBP2 transcript variant 7	NM_001300990.2:c.1016-1580=	NM_001300990.2:c.1016-1580T>A	NM_001300990.2:c.1016-1580T>C
PTBP2 transcript	NM_021190.2:c.1172-1580=	NM_021190.2:c.1172-1580T>A	NM_021190.2:c.1172-1580T>C
PTBP2 transcript variant 6	NM_021190.4:c.1172-1580=	NM_021190.4:c.1172-1580T>A	NM_021190.4:c.1172-1580T>C
PTBP2 transcript variant X1	XM_005271084.1:c.1187-1580=	XM_005271084.1:c.1187-1580T>A	XM_005271084.1:c.1187-1580T>C
PTBP2 transcript variant X2	XM_005271085.1:c.1187-1580=	XM_005271085.1:c.1187-1580T>A	XM_005271085.1:c.1187-1580T>C
PTBP2 transcript variant X3	XM_005271086.1:c.1172-1580=	XM_005271086.1:c.1172-1580T>A	XM_005271086.1:c.1172-1580T>C
PTBP2 transcript variant X2	XM_011541874.3:c.1211-1580=	XM_011541874.3:c.1211-1580T>A	XM_011541874.3:c.1211-1580T>C
PTBP2 transcript variant X3	XM_011541875.3:c.1196-1580=	XM_011541875.3:c.1196-1580T>A	XM_011541875.3:c.1196-1580T>C
PTBP2 transcript variant X1	XM_011541876.3:c.1211-1580=	XM_011541876.3:c.1211-1580T>A	XM_011541876.3:c.1211-1580T>C
PTBP2 transcript variant X6	XM_017001951.2:c.1220-1580=	XM_017001951.2:c.1220-1580T>A	XM_017001951.2:c.1220-1580T>C
PTBP2 transcript variant X3	XM_047426537.1:c.1094-1580=	XM_047426537.1:c.1094-1580T>A	XM_047426537.1:c.1094-1580T>C

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#.

73 SubSNP, 20 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	KWOK	ss355835	Jul 12, 2000 (79)
2	SC_JCM	ss821201	Aug 11, 2000 (85)
3	KWOK	ss1131997	Oct 04, 2000 (86)
4	KWOK	ss1132730	Oct 04, 2000 (86)
5	KWOK	ss1133181	Oct 04, 2000 (86)
6	KWOK	ss1794742	Oct 18, 2000 (87)
7	KWOK	ss1795149	Oct 18, 2000 (87)
8	CSHL-HAPMAP	ss19871287	Feb 27, 2004 (120)
9	SSAHASNP	ss20572221	Apr 05, 2004 (121)
10	ABI	ss44007186	Mar 14, 2006 (126)
11	HGSV	ss77744084	Dec 07, 2007 (129)
12	KRIBB_YJKIM	ss80750587	Dec 15, 2007 (130)
13	HUMANGENOME_JCVI	ss99231263	Feb 06, 2009 (130)
14	1000GENOMES	ss108438186	Jan 23, 2009 (130)
15	ENSEMBL	ss138847279	Dec 01, 2009 (131)
16	GMI	ss155389649	Dec 01, 2009 (131)
17	BUSHMAN	ss198811658	Jul 04, 2010 (132)
18	1000GENOMES	ss230649315	Jul 14, 2010 (132)
19	1000GENOMES	ss238318431	Jul 15, 2010 (132)
20	GMI	ss275938774	May 04, 2012 (137)
21	PJP	ss290577202	May 09, 2011 (134)
22	TISHKOFF	ss554463040	Apr 25, 2013 (138)
23	SSMP	ss648240962	Apr 25, 2013 (138)
24	EVA-GONL	ss975462534	Aug 21, 2014 (142)
25	JMKIDD_LAB	ss1068113226	Aug 21, 2014 (142)
26	1000GENOMES	ss1292031488	Aug 21, 2014 (142)
27	DDI	ss1425906156	Apr 01, 2015 (144)
28	EVA_GENOME_DK	ss1574256617	Apr 01, 2015 (144)
29	EVA_DECODE	ss1584839801	Apr 01, 2015 (144)
30	EVA_UK10K_ALSPAC	ss1600775361	Apr 01, 2015 (144)
31	EVA_UK10K_TWINSUK	ss1643769394	Apr 01, 2015 (144)
32	HAMMER_LAB	ss1794782798	Sep 08, 2015 (146)
33	WEILL_CORNELL_DGM	ss1918663279	Feb 12, 2016 (147)
34	GENOMED	ss1966816440	Jul 19, 2016 (147)
35	JJLAB	ss2019852935	Sep 14, 2016 (149)
36	USC_VALOUEV	ss2147871750	Dec 20, 2016 (150)
37	HUMAN_LONGEVITY	ss2164865651	Dec 20, 2016 (150)
38	SYSTEMSBIOZJU	ss2624438371	Nov 08, 2017 (151)
39	GRF	ss2697798844	Nov 08, 2017 (151)
40	GNOMAD	ss2758415897	Nov 08, 2017 (151)
41	AFFY	ss2984868175	Nov 08, 2017 (151)
42	AFFY	ss2985519601	Nov 08, 2017 (151)
43	SWEGEN	ss2987275312	Nov 08, 2017 (151)
44	BIOINF_KMB_FNS_UNIBA	ss3023690132	Nov 08, 2017 (151)
45	CSHL	ss3343587312	Nov 08, 2017 (151)
46	URBANLAB	ss3646727784	Oct 11, 2018 (152)
47	ILLUMINA	ss3653640032	Oct 11, 2018 (152)
48	EGCUT_WGS	ss3655357367	Jul 12, 2019 (153)
49	EVA_DECODE	ss3687330269	Jul 12, 2019 (153)
50	ACPOP	ss3727297387	Jul 12, 2019 (153)
51	EVA	ss3746551676	Jul 12, 2019 (153)
52	PACBIO	ss3783491577	Jul 12, 2019 (153)
53	PACBIO	ss3789137340	Jul 12, 2019 (153)
54	PACBIO	ss3794010179	Jul 12, 2019 (153)
55	KHV_HUMAN_GENOMES	ss3799553434	Jul 12, 2019 (153)
56	EVA	ss3826317492	Apr 25, 2020 (154)
57	SGDP_PRJ	ss3849439562	Apr 25, 2020 (154)
58	KRGDB	ss3894513092	Apr 25, 2020 (154)
59	KOGIC	ss3945057738	Apr 25, 2020 (154)
60	TOPMED	ss4459985775	Apr 25, 2021 (155)
61	TOMMO_GENOMICS	ss5145228543	Apr 25, 2021 (155)
62	1000G_HIGH_COVERAGE	ss5243257304	Oct 12, 2022 (156)
63	EVA	ss5320549584	Oct 12, 2022 (156)
64	HUGCELL_USP	ss5444215685	Oct 12, 2022 (156)
65	EVA	ss5505959071	Oct 12, 2022 (156)
66	1000G_HIGH_COVERAGE	ss5516061553	Oct 12, 2022 (156)
67	SANFORD_IMAGENETICS	ss5626095713	Oct 12, 2022 (156)
68	TOMMO_GENOMICS	ss5670364487	Oct 12, 2022 (156)
69	YY_MCH	ss5800844404	Oct 12, 2022 (156)
70	EVA	ss5832346400	Oct 12, 2022 (156)
71	EVA	ss5849026459	Oct 12, 2022 (156)
72	EVA	ss5909397348	Oct 12, 2022 (156)
73	EVA	ss5937953498	Oct 12, 2022 (156)
74	1000Genomes	NC_000001.10 - 97276688	Oct 11, 2018 (152)
75	1000Genomes_30x	NC_000001.11 - 96811132	Oct 12, 2022 (156)
76	The Avon Longitudinal Study of Parents and Children	NC_000001.10 - 97276688	Oct 11, 2018 (152)
77	Genetic variation in the Estonian population	NC_000001.10 - 97276688	Oct 11, 2018 (152)
78	The Danish reference pan genome	NC_000001.10 - 97276688	Apr 25, 2020 (154)
79	gnomAD - Genomes	NC_000001.11 - 96811132	Apr 25, 2021 (155)
80	Genome of the Netherlands Release 5	NC_000001.10 - 97276688	Apr 25, 2020 (154)
81	HapMap	NC_000001.11 - 96811132	Apr 25, 2020 (154)
82	KOREAN population from KRGDB	NC_000001.10 - 97276688	Apr 25, 2020 (154)
83	Korean Genome Project	NC_000001.11 - 96811132	Apr 25, 2020 (154)
84	Northern Sweden	NC_000001.10 - 97276688	Jul 12, 2019 (153)
85	Qatari	NC_000001.10 - 97276688	Apr 25, 2020 (154)
86	SGDP_PRJ	NC_000001.10 - 97276688	Apr 25, 2020 (154)
87	Siberian	NC_000001.10 - 97276688	Apr 25, 2020 (154)
88	8.3KJPN	NC_000001.10 - 97276688	Apr 25, 2021 (155)
89	14KJPN	NC_000001.11 - 96811132	Oct 12, 2022 (156)
90	TopMed	NC_000001.11 - 96811132	Apr 25, 2021 (155)
91	UK 10K study - Twins	NC_000001.10 - 97276688	Oct 11, 2018 (152)
92	A Vietnamese Genetic Variation Database	NC_000001.10 - 97276688	Jul 12, 2019 (153)
93	ALFA	NC_000001.11 - 96811132	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)
rs648292	Sep 19, 2000 (85)
rs60232958	May 25, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
1690486, ss3894513092	NC_000001.10:97276687:T:A	NC_000001.11:96811131:T:A	(self)
464705640	NC_000001.11:96811131:T:A	NC_000001.11:96811131:T:A	(self)
ss77744084	NC_000001.8:96988708:T:C	NC_000001.11:96811131:T:C	(self)
ss108438186, ss198811658, ss275938774, ss290577202, ss1584839801	NC_000001.9:97049275:T:C	NC_000001.11:96811131:T:C	(self)
2792502, 1538542, 1095615, 1620878, 667020, 1690486, 582252, 705209, 1456542, 388104, 3197850, 1538542, 331077, ss230649315, ss238318431, ss554463040, ss648240962, ss975462534, ss1068113226, ss1292031488, ss1425906156, ss1574256617, ss1600775361, ss1643769394, ss1794782798, ss1918663279, ss1966816440, ss2019852935, ss2147871750, ss2624438371, ss2697798844, ss2758415897, ss2984868175, ss2985519601, ss2987275312, ss3343587312, ss3653640032, ss3655357367, ss3727297387, ss3746551676, ss3783491577, ss3789137340, ss3794010179, ss3826317492, ss3849439562, ss3894513092, ss5145228543, ss5320549584, ss5505959071, ss5626095713, ss5832346400, ss5937953498	NC_000001.10:97276687:T:C	NC_000001.11:96811131:T:C	(self)
3587488, 19725220, 132523, 1435739, 4201591, 23592110, 464705640, ss2164865651, ss3023690132, ss3646727784, ss3687330269, ss3799553434, ss3945057738, ss4459985775, ss5243257304, ss5444215685, ss5516061553, ss5670364487, ss5800844404, ss5849026459, ss5909397348	NC_000001.11:96811131:T:C	NC_000001.11:96811131:T:C	(self)
ss19871287, ss20572221	NT_028050.13:5474509:T:C	NC_000001.11:96811131:T:C	(self)
ss355835, ss821201, ss1131997, ss1132730, ss1133181, ss1794742, ss1795149, ss44007186, ss80750587, ss99231263, ss138847279, ss155389649	NT_032977.9:67248605:T:C	NC_000001.11:96811131: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 rs273882

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

rs273882