Name: rs1130941
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.

rs1130941

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr13:24459062 (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
Variation Type: SNV Single Nucleotide Variation
Frequency: A=0.116344 (30795/264690, TOPMED)
A=0.094308 (23513/249322, GnomAD_exome)
A=0.122254 (17139/140192, GnomAD) (+ 23 more)
A=0.098553 (11767/119398, ExAC)
A=0.11564 (5841/50510, ALFA)
A=0.00598 (169/28258, 14KJPN)
A=0.00638 (107/16760, 8.3KJPN)
A=0.13038 (1695/13000, GO-ESP)
A=0.0899 (576/6404, 1000G_30x)
A=0.0907 (454/5008, 1000G)
A=0.1263 (566/4480, Estonian)
A=0.1318 (508/3854, ALSPAC)
A=0.1197 (444/3708, TWINSUK)
A=0.0116 (34/2930, KOREAN)
A=0.0131 (24/1832, Korea1K)
A=0.108 (108/998, GoNL)
A=0.034 (21/614, Vietnamese)
A=0.130 (78/600, NorthernSweden)
A=0.103 (55/534, MGP)
A=0.074 (24/324, HapMap)
A=0.115 (35/304, FINRISK)
A=0.125 (27/216, Qatari)
T=0.500 (51/102, SGDP_PRJ)
A=0.500 (51/102, SGDP_PRJ)
A=0.17 (7/40, GENOME_DK)
T=0.45 (9/20, Siberian)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: PARP4 : Synonymous 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	50510	T=0.88436	A=0.11564
European	Sub	38444	T=0.88341	A=0.11659
African	Sub	3574	T=0.8590	A=0.1410
African Others	Sub	122	T=0.844	A=0.156
African American	Sub	3452	T=0.8595	A=0.1405
Asian	Sub	168	T=0.970	A=0.030
East Asian	Sub	112	T=0.964	A=0.036
Other Asian	Sub	56	T=0.98	A=0.02
Latin American 1	Sub	500	T=0.868	A=0.132
Latin American 2	Sub	628	T=0.941	A=0.059
South Asian	Sub	98	T=0.93	A=0.07
Other	Sub	7098	T=0.8957	A=0.1043

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=0.883656	A=0.116344
gnomAD - Exomes	Global	Study-wide	249322	T=0.905692	A=0.094308
gnomAD - Exomes	European	Sub	134476	T=0.883697	A=0.116303
gnomAD - Exomes	Asian	Sub	48578	T=0.94903	A=0.05097
gnomAD - Exomes	American	Sub	34116	T=0.94982	A=0.05018
gnomAD - Exomes	African	Sub	16040	T=0.84401	A=0.15599
gnomAD - Exomes	Ashkenazi Jewish	Sub	10026	T=0.94484	A=0.05516
gnomAD - Exomes	Other	Sub	6086	T=0.8965	A=0.1035
gnomAD - Genomes	Global	Study-wide	140192	T=0.877746	A=0.122254
gnomAD - Genomes	European	Sub	75934	T=0.88102	A=0.11898
gnomAD - Genomes	African	Sub	42002	T=0.84648	A=0.15352
gnomAD - Genomes	American	Sub	13646	T=0.91331	A=0.08669
gnomAD - Genomes	Ashkenazi Jewish	Sub	3324	T=0.9458	A=0.0542
gnomAD - Genomes	East Asian	Sub	3134	T=0.9796	A=0.0204
gnomAD - Genomes	Other	Sub	2152	T=0.8936	A=0.1064
ExAC	Global	Study-wide	119398	T=0.901447	A=0.098553
ExAC	Europe	Sub	72274	T=0.88656	A=0.11344
ExAC	Asian	Sub	24836	T=0.94838	A=0.05162
ExAC	American	Sub	11398	T=0.95034	A=0.04966
ExAC	African	Sub	10000	T=0.8365	A=0.1635
ExAC	Other	Sub	890	T=0.904	A=0.096
Allele Frequency Aggregator	Total	Global	50510	T=0.88436	A=0.11564
Allele Frequency Aggregator	European	Sub	38444	T=0.88341	A=0.11659
Allele Frequency Aggregator	Other	Sub	7098	T=0.8957	A=0.1043
Allele Frequency Aggregator	African	Sub	3574	T=0.8590	A=0.1410
Allele Frequency Aggregator	Latin American 2	Sub	628	T=0.941	A=0.059
Allele Frequency Aggregator	Latin American 1	Sub	500	T=0.868	A=0.132
Allele Frequency Aggregator	Asian	Sub	168	T=0.970	A=0.030
Allele Frequency Aggregator	South Asian	Sub	98	T=0.93	A=0.07
14KJPN	JAPANESE	Study-wide	28258	T=0.99402	A=0.00598
8.3KJPN	JAPANESE	Study-wide	16760	T=0.99362	A=0.00638
GO Exome Sequencing Project	Global	Study-wide	13000	T=0.86962	A=0.13038
GO Exome Sequencing Project	European American	Sub	8600	T=0.8844	A=0.1156
GO Exome Sequencing Project	African American	Sub	4400	T=0.8407	A=0.1593
1000Genomes_30x	Global	Study-wide	6404	T=0.9101	A=0.0899
1000Genomes_30x	African	Sub	1786	T=0.8371	A=0.1629
1000Genomes_30x	Europe	Sub	1266	T=0.9107	A=0.0893
1000Genomes_30x	South Asian	Sub	1202	T=0.9476	A=0.0524
1000Genomes_30x	East Asian	Sub	1170	T=0.9667	A=0.0333
1000Genomes_30x	American	Sub	980	T=0.929	A=0.071
1000Genomes	Global	Study-wide	5008	T=0.9093	A=0.0907
1000Genomes	African	Sub	1322	T=0.8298	A=0.1702
1000Genomes	East Asian	Sub	1008	T=0.9683	A=0.0317
1000Genomes	Europe	Sub	1006	T=0.9066	A=0.0934
1000Genomes	South Asian	Sub	978	T=0.946	A=0.054
1000Genomes	American	Sub	694	T=0.928	A=0.072
Genetic variation in the Estonian population	Estonian	Study-wide	4480	T=0.8737	A=0.1263
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	T=0.8682	A=0.1318
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	T=0.8803	A=0.1197
KOREAN population from KRGDB	KOREAN	Study-wide	2930	T=0.9884	A=0.0116
Korean Genome Project	KOREAN	Study-wide	1832	T=0.9869	A=0.0131
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	T=0.892	A=0.108
A Vietnamese Genetic Variation Database	Global	Study-wide	614	T=0.966	A=0.034
Northern Sweden	ACPOP	Study-wide	600	T=0.870	A=0.130
Medical Genome Project healthy controls from Spanish population	Spanish controls	Study-wide	534	T=0.897	A=0.103
HapMap	Global	Study-wide	324	T=0.926	A=0.074
HapMap	African	Sub	118	T=0.881	A=0.119
HapMap	American	Sub	116	T=0.914	A=0.086
HapMap	Asian	Sub	90	T=1.00	A=0.00
FINRISK	Finnish from FINRISK project	Study-wide	304	T=0.885	A=0.115
Qatari	Global	Study-wide	216	T=0.875	A=0.125
SGDP_PRJ	Global	Study-wide	102	T=0.500	A=0.500
The Danish reference pan genome	Danish	Study-wide	40	T=0.82	A=0.17
Siberian	Global	Study-wide	20	T=0.45	A=0.55

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 13	NC_000013.11:g.24459062T>A
GRCh37.p13 chr 13	NC_000013.10:g.25033200T>A

Gene: PARP4, poly(ADP-ribose) polymerase family member 4 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
PARP4 transcript	NM_006437.4:c.2406A>T	T [ACA] > T [ACT]	Coding Sequence Variant
protein mono-ADP-ribosyltransferase PARP4	NP_006428.2:p.Thr802=	T (Thr) > T (Thr)	Synonymous Variant
PARP4 transcript variant X1	XM_011534932.3:c.2406A>T	T [ACA] > T [ACT]	Coding Sequence Variant
protein mono-ADP-ribosyltransferase PARP4 isoform X1	XP_011533234.1:p.Thr802=	T (Thr) > T (Thr)	Synonymous Variant
PARP4 transcript variant X2	XM_047430097.1:c.2406A>T	T [ACA] > T [ACT]	Coding Sequence Variant
protein mono-ADP-ribosyltransferase PARP4 isoform X1	XP_047286053.1:p.Thr802=	T (Thr) > T (Thr)	Synonymous 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
GRCh38.p14 chr 13	NC_000013.11:g.24459062=	NC_000013.11:g.24459062T>A
GRCh37.p13 chr 13	NC_000013.10:g.25033200=	NC_000013.10:g.25033200T>A
PARP4 transcript	NM_006437.4:c.2406=	NM_006437.4:c.2406A>T
PARP4 transcript	NM_006437.3:c.2406=	NM_006437.3:c.2406A>T
PARP4 transcript variant X1	XM_011534932.3:c.2406=	XM_011534932.3:c.2406A>T
PARP4 transcript variant X2	XM_011534932.2:c.2406=	XM_011534932.2:c.2406A>T
PARP4 transcript variant X2	XM_011534932.1:c.2406=	XM_011534932.1:c.2406A>T
PARP4 transcript variant X2	XM_047430097.1:c.2406=	XM_047430097.1:c.2406A>T
protein mono-ADP-ribosyltransferase PARP4	NP_006428.2:p.Thr802=	NP_006428.2:p.Thr802=
protein mono-ADP-ribosyltransferase PARP4 isoform X1	XP_011533234.1:p.Thr802=	XP_011533234.1:p.Thr802=
protein mono-ADP-ribosyltransferase PARP4 isoform X1	XP_047286053.1:p.Thr802=	XP_047286053.1:p.Thr802=

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#.

82 SubSNP, 25 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	SNP500CANCER	ss5586210	Jul 02, 2003 (130)
2	SC_SNP	ss13307181	Dec 05, 2003 (130)
3	PERLEGEN	ss23434433	Sep 20, 2004 (130)
4	CORNELL	ss86238023	Mar 23, 2008 (129)
5	1000GENOMES	ss112617753	Feb 14, 2009 (130)
6	1000GENOMES	ss114418758	Jan 25, 2009 (130)
7	SEATTLESEQ	ss159727883	Dec 01, 2009 (131)
8	ILLUMINA	ss160771127	Dec 01, 2009 (131)
9	COMPLETE_GENOMICS	ss168972285	Jul 04, 2010 (132)
10	BUSHMAN	ss198973416	Jul 04, 2010 (132)
11	1000GENOMES	ss226080376	Jul 14, 2010 (132)
12	1000GENOMES	ss236176667	Jul 15, 2010 (132)
13	BL	ss254854106	May 09, 2011 (134)
14	GMI	ss286668403	Apr 25, 2013 (138)
15	NHLBI-ESP	ss342373225	May 09, 2011 (134)
16	ILLUMINA	ss482243255	Sep 08, 2015 (146)
17	1000GENOMES	ss491056946	May 04, 2012 (137)
18	CLINSEQ_SNP	ss491677239	May 04, 2012 (137)
19	ILLUMINA	ss536086157	Sep 08, 2015 (146)
20	TISHKOFF	ss563550314	Apr 25, 2013 (138)
21	SSMP	ss659144296	Apr 25, 2013 (138)
22	JMKIDD_LAB	ss974486231	Aug 21, 2014 (142)
23	EVA-GONL	ss990193026	Aug 21, 2014 (142)
24	JMKIDD_LAB	ss1067540208	Aug 21, 2014 (142)
25	JMKIDD_LAB	ss1078937865	Aug 21, 2014 (142)
26	1000GENOMES	ss1347495619	Aug 21, 2014 (142)
27	EVA_GENOME_DK	ss1576672815	Apr 01, 2015 (144)
28	EVA_FINRISK	ss1584086126	Apr 01, 2015 (144)
29	EVA_UK10K_ALSPAC	ss1629890266	Apr 01, 2015 (144)
30	EVA_DECODE	ss1642298483	Apr 01, 2015 (144)
31	EVA_UK10K_TWINSUK	ss1672884299	Apr 01, 2015 (144)
32	EVA_EXAC	ss1691227686	Apr 01, 2015 (144)
33	EVA_MGP	ss1711352390	Apr 01, 2015 (144)
34	HAMMER_LAB	ss1807525992	Sep 08, 2015 (146)
35	WEILL_CORNELL_DGM	ss1933561392	Feb 12, 2016 (147)
36	JJLAB	ss2027535094	Sep 14, 2016 (149)
37	USC_VALOUEV	ss2155898949	Dec 20, 2016 (150)
38	HUMAN_LONGEVITY	ss2194862418	Dec 20, 2016 (150)
39	GNOMAD	ss2740317765	Nov 08, 2017 (151)
40	GNOMAD	ss2749018793	Nov 08, 2017 (151)
41	GNOMAD	ss2917600791	Nov 08, 2017 (151)
42	SWEGEN	ss3010721453	Nov 08, 2017 (151)
43	BIOINF_KMB_FNS_UNIBA	ss3027582316	Nov 08, 2017 (151)
44	CSHL	ss3350365095	Nov 08, 2017 (151)
45	ILLUMINA	ss3627021892	Oct 12, 2018 (152)
46	ILLUMINA	ss3636222160	Oct 12, 2018 (152)
47	OMUKHERJEE_ADBS	ss3646451581	Oct 12, 2018 (152)
48	EGCUT_WGS	ss3677985755	Jul 13, 2019 (153)
49	EVA_DECODE	ss3694926050	Jul 13, 2019 (153)
50	ACPOP	ss3739582497	Jul 13, 2019 (153)
51	EVA	ss3751236041	Jul 13, 2019 (153)
52	PACBIO	ss3787404018	Jul 13, 2019 (153)
53	PACBIO	ss3792477939	Jul 13, 2019 (153)
54	PACBIO	ss3797361646	Jul 13, 2019 (153)
55	KHV_HUMAN_GENOMES	ss3816567032	Jul 13, 2019 (153)
56	EVA	ss3824796675	Apr 27, 2020 (154)
57	EVA	ss3825834042	Apr 27, 2020 (154)
58	EVA	ss3833448304	Apr 27, 2020 (154)
59	EVA	ss3840299978	Apr 27, 2020 (154)
60	EVA	ss3845784448	Apr 27, 2020 (154)
61	SGDP_PRJ	ss3879593614	Apr 27, 2020 (154)
62	KRGDB	ss3928410550	Apr 27, 2020 (154)
63	KOGIC	ss3973207709	Apr 27, 2020 (154)
64	FSA-LAB	ss3984043725	Apr 26, 2021 (155)
65	EVA	ss3986596677	Apr 26, 2021 (155)
66	TOPMED	ss4939954302	Apr 26, 2021 (155)
67	TOMMO_GENOMICS	ss5209178048	Apr 26, 2021 (155)
68	EVA	ss5236911772	Apr 26, 2021 (155)
69	1000G_HIGH_COVERAGE	ss5293097271	Oct 16, 2022 (156)
70	EVA	ss5409609580	Oct 16, 2022 (156)
71	HUGCELL_USP	ss5487524475	Oct 16, 2022 (156)
72	EVA	ss5510907618	Oct 16, 2022 (156)
73	1000G_HIGH_COVERAGE	ss5591732390	Oct 16, 2022 (156)
74	EVA	ss5623960075	Oct 16, 2022 (156)
75	EVA	ss5624039365	Oct 16, 2022 (156)
76	SANFORD_IMAGENETICS	ss5654401829	Oct 16, 2022 (156)
77	TOMMO_GENOMICS	ss5760820012	Oct 16, 2022 (156)
78	YY_MCH	ss5813950004	Oct 16, 2022 (156)
79	EVA	ss5839222028	Oct 16, 2022 (156)
80	EVA	ss5848369795	Oct 16, 2022 (156)
81	EVA	ss5924371380	Oct 16, 2022 (156)
82	EVA	ss5945806780	Oct 16, 2022 (156)
83	1000Genomes	NC_000013.10 - 25033200	Oct 12, 2018 (152)
84	1000Genomes_30x	NC_000013.11 - 24459062	Oct 16, 2022 (156)
85	The Avon Longitudinal Study of Parents and Children	NC_000013.10 - 25033200	Oct 12, 2018 (152)
86	Genetic variation in the Estonian population	NC_000013.10 - 25033200	Oct 12, 2018 (152)
87	ExAC	NC_000013.10 - 25033200	Oct 12, 2018 (152)
88	FINRISK	NC_000013.10 - 25033200	Apr 27, 2020 (154)
89	The Danish reference pan genome	NC_000013.10 - 25033200	Apr 27, 2020 (154)
90	gnomAD - Genomes	NC_000013.11 - 24459062	Apr 26, 2021 (155)
91	gnomAD - Exomes	NC_000013.10 - 25033200	Jul 13, 2019 (153)
92	GO Exome Sequencing Project	NC_000013.10 - 25033200	Oct 12, 2018 (152)
93	Genome of the Netherlands Release 5	NC_000013.10 - 25033200	Apr 27, 2020 (154)
94	HapMap	NC_000013.11 - 24459062	Apr 27, 2020 (154)
95	KOREAN population from KRGDB	NC_000013.10 - 25033200	Apr 27, 2020 (154)
96	Korean Genome Project	NC_000013.11 - 24459062	Apr 27, 2020 (154)
97	Medical Genome Project healthy controls from Spanish population	NC_000013.10 - 25033200	Apr 27, 2020 (154)
98	Northern Sweden	NC_000013.10 - 25033200	Jul 13, 2019 (153)
99	Qatari	NC_000013.10 - 25033200	Apr 27, 2020 (154)
100	SGDP_PRJ	NC_000013.10 - 25033200	Apr 27, 2020 (154)
101	Siberian	NC_000013.10 - 25033200	Apr 27, 2020 (154)
102	8.3KJPN	NC_000013.10 - 25033200	Apr 26, 2021 (155)
103	14KJPN	NC_000013.11 - 24459062	Oct 16, 2022 (156)
104	TopMed	NC_000013.11 - 24459062	Apr 26, 2021 (155)
105	UK 10K study - Twins	NC_000013.10 - 25033200	Oct 12, 2018 (152)
106	A Vietnamese Genetic Variation Database	NC_000013.10 - 25033200	Jul 13, 2019 (153)
107	ALFA	NC_000013.11 - 24459062	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)
rs3190389	Oct 09, 2002 (108)
rs6413414	May 23, 2008 (130)
rs17413352	May 23, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss112617753, ss114418758, ss168972285, ss198973416, ss254854106, ss286668403, ss491677239, ss1642298483	NC_000013.9:23931199:T:A	NC_000013.11:24459061:T:A	(self)
60339046, 33509712, 23724003, 1551318, 82587, 3220129, 9559202, 1254068, 14950576, 35587944, 468150, 12867362, 15603322, 31610594, 8415303, 67147355, 33509712, 7433169, ss226080376, ss236176667, ss342373225, ss482243255, ss491056946, ss536086157, ss563550314, ss659144296, ss974486231, ss990193026, ss1067540208, ss1078937865, ss1347495619, ss1576672815, ss1584086126, ss1629890266, ss1672884299, ss1691227686, ss1711352390, ss1807525992, ss1933561392, ss2027535094, ss2155898949, ss2740317765, ss2749018793, ss2917600791, ss3010721453, ss3350365095, ss3627021892, ss3636222160, ss3646451581, ss3677985755, ss3739582497, ss3751236041, ss3787404018, ss3792477939, ss3797361646, ss3824796675, ss3825834042, ss3833448304, ss3840299978, ss3879593614, ss3928410550, ss3984043725, ss3986596677, ss5209178048, ss5409609580, ss5510907618, ss5623960075, ss5624039365, ss5654401829, ss5839222028, ss5848369795, ss5945806780	NC_000013.10:25033199:T:A	NC_000013.11:24459061:T:A	(self)
79258325, 425515104, 948138, 29585710, 94657116, 155499960, 15004714976, ss2194862418, ss3027582316, ss3694926050, ss3816567032, ss3845784448, ss3973207709, ss4939954302, ss5236911772, ss5293097271, ss5487524475, ss5591732390, ss5760820012, ss5813950004, ss5924371380	NC_000013.11:24459061:T:A	NC_000013.11:24459061:T:A	(self)
ss13307181	NT_009799.12:6013199:T:A	NC_000013.11:24459061:T:A	(self)
ss5586210, ss23434433, ss86238023, ss159727883, ss160771127	NT_024524.14:6013199:T:A	NC_000013.11:24459061:T:A	(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 rs1130941

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

rs1130941