Name: rs14083
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.

rs14083

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr12:20683922 (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: A>C / A>G / A>T
Variation Type: SNV Single Nucleotide Variation
Frequency: A=0.311855 (82545/264690, TOPMED)
A=0.306169 (42863/139998, GnomAD)
A=0.317310 (37652/118660, ALFA) (+ 19 more)
A=0.31524 (24810/78702, PAGE_STUDY)
A=0.17245 (4873/28258, 14KJPN)
A=0.17190 (2881/16760, 8.3KJPN)
A=0.2800 (1793/6404, 1000G_30x)
A=0.2780 (1392/5008, 1000G)
A=0.3179 (1424/4480, Estonian)
A=0.3241 (1249/3854, ALSPAC)
A=0.3255 (1207/3708, TWINSUK)
A=0.1457 (427/2930, KOREAN)
A=0.1501 (275/1832, Korea1K)
A=0.347 (346/998, GoNL)
A=0.144 (114/790, PRJEB37584)
A=0.373 (224/600, NorthernSweden)
A=0.218 (103/472, SGDP_PRJ)
A=0.236 (51/216, Qatari)
A=0.162 (35/216, Vietnamese)
A=0.26 (13/50, Siberian)
A=0.22 (10/46, Ancient Sardinia)
A=0.40 (16/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: PDE3A : 3 Prime UTR 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	123696	A=0.317197	G=0.682803, T=0.000000
European	Sub	105402	A=0.314719	G=0.685281, T=0.000000
African	Sub	5222	A=0.2771	G=0.7229, T=0.0000
African Others	Sub	206	A=0.262	G=0.738, T=0.000
African American	Sub	5016	A=0.2777	G=0.7223, T=0.0000
Asian	Sub	3576	A=0.1751	G=0.8249, T=0.0000
East Asian	Sub	2920	A=0.1432	G=0.8568, T=0.0000
Other Asian	Sub	656	A=0.317	G=0.683, T=0.000
Latin American 1	Sub	528	A=0.290	G=0.710, T=0.000
Latin American 2	Sub	5078	A=0.5289	G=0.4711, T=0.0000
South Asian	Sub	298	A=0.289	G=0.711, T=0.000
Other	Sub	3592	A=0.2968	G=0.7032, T=0.0000

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	A=0.311855	G=0.688145
gnomAD - Genomes	Global	Study-wide	139998	A=0.306169	G=0.693831
gnomAD - Genomes	European	Sub	75848	A=0.31450	G=0.68550
gnomAD - Genomes	African	Sub	41924	A=0.27082	G=0.72918
gnomAD - Genomes	American	Sub	13620	A=0.42548	G=0.57452
gnomAD - Genomes	Ashkenazi Jewish	Sub	3322	A=0.1933	G=0.8067
gnomAD - Genomes	East Asian	Sub	3130	A=0.1754	G=0.8246
gnomAD - Genomes	Other	Sub	2154	A=0.3106	G=0.6894
Allele Frequency Aggregator	Total	Global	118660	A=0.317310	G=0.682690, T=0.000000
Allele Frequency Aggregator	European	Sub	102308	A=0.314521	G=0.685479, T=0.000000
Allele Frequency Aggregator	Latin American 2	Sub	5078	A=0.5289	G=0.4711, T=0.0000
Allele Frequency Aggregator	African	Sub	4080	A=0.2718	G=0.7282, T=0.0000
Allele Frequency Aggregator	Asian	Sub	3576	A=0.1751	G=0.8249, T=0.0000
Allele Frequency Aggregator	Other	Sub	2792	A=0.2915	G=0.7085, T=0.0000
Allele Frequency Aggregator	Latin American 1	Sub	528	A=0.290	G=0.710, T=0.000
Allele Frequency Aggregator	South Asian	Sub	298	A=0.289	G=0.711, T=0.000
The PAGE Study	Global	Study-wide	78702	A=0.31524	G=0.68476
The PAGE Study	AfricanAmerican	Sub	32516	A=0.27451	G=0.72549
The PAGE Study	Mexican	Sub	10810	A=0.50518	G=0.49482
The PAGE Study	Asian	Sub	8318	A=0.1603	G=0.8397
The PAGE Study	PuertoRican	Sub	7918	A=0.3625	G=0.6375
The PAGE Study	NativeHawaiian	Sub	4534	A=0.2408	G=0.7592
The PAGE Study	Cuban	Sub	4230	A=0.2799	G=0.7201
The PAGE Study	Dominican	Sub	3828	A=0.3020	G=0.6980
The PAGE Study	CentralAmerican	Sub	2450	A=0.4371	G=0.5629
The PAGE Study	SouthAmerican	Sub	1982	A=0.5010	G=0.4990
The PAGE Study	NativeAmerican	Sub	1260	A=0.4008	G=0.5992
The PAGE Study	SouthAsian	Sub	856	A=0.256	G=0.744
14KJPN	JAPANESE	Study-wide	28258	A=0.17245	G=0.82755
8.3KJPN	JAPANESE	Study-wide	16760	A=0.17190	G=0.82810
1000Genomes_30x	Global	Study-wide	6404	A=0.2800	G=0.7200
1000Genomes_30x	African	Sub	1786	A=0.2592	G=0.7408
1000Genomes_30x	Europe	Sub	1266	A=0.2859	G=0.7141
1000Genomes_30x	South Asian	Sub	1202	A=0.2562	G=0.7438
1000Genomes_30x	East Asian	Sub	1170	A=0.1889	G=0.8111
1000Genomes_30x	American	Sub	980	A=0.448	G=0.552
1000Genomes	Global	Study-wide	5008	A=0.2780	G=0.7220
1000Genomes	African	Sub	1322	A=0.2640	G=0.7360
1000Genomes	East Asian	Sub	1008	A=0.1885	G=0.8115
1000Genomes	Europe	Sub	1006	A=0.2813	G=0.7187
1000Genomes	South Asian	Sub	978	A=0.263	G=0.737
1000Genomes	American	Sub	694	A=0.451	G=0.549
Genetic variation in the Estonian population	Estonian	Study-wide	4480	A=0.3179	G=0.6821
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	A=0.3241	G=0.6759
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	A=0.3255	G=0.6745
KOREAN population from KRGDB	KOREAN	Study-wide	2930	A=0.1457	C=0.0000, G=0.8543, T=0.0000
Korean Genome Project	KOREAN	Study-wide	1832	A=0.1501	G=0.8499
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	A=0.347	G=0.653
CNV burdens in cranial meningiomas	Global	Study-wide	790	A=0.144	G=0.856
CNV burdens in cranial meningiomas	CRM	Sub	790	A=0.144	G=0.856
Northern Sweden	ACPOP	Study-wide	600	A=0.373	G=0.627
SGDP_PRJ	Global	Study-wide	472	A=0.218	G=0.782
Qatari	Global	Study-wide	216	A=0.236	G=0.764
A Vietnamese Genetic Variation Database	Global	Study-wide	216	A=0.162	G=0.838
Siberian	Global	Study-wide	50	A=0.26	G=0.74
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	46	A=0.22	G=0.78
The Danish reference pan genome	Danish	Study-wide	40	A=0.40	G=0.60

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 12	NC_000012.12:g.20683922A>C
GRCh38.p14 chr 12	NC_000012.12:g.20683922A>G
GRCh38.p14 chr 12	NC_000012.12:g.20683922A>T
GRCh37.p13 chr 12	NC_000012.11:g.20836856A>C
GRCh37.p13 chr 12	NC_000012.11:g.20836856A>G
GRCh37.p13 chr 12	NC_000012.11:g.20836856A>T
PDE3A RefSeqGene	NG_030033.1:g.319678A>C
PDE3A RefSeqGene	NG_030033.1:g.319678A>G
PDE3A RefSeqGene	NG_030033.1:g.319678A>T

Gene: PDE3A, phosphodiesterase 3A (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
PDE3A transcript variant 2	NM_001244683.2:c.*3651=	N/A	3 Prime UTR Variant
PDE3A transcript variant 4	NM_001378408.1:c.*3805=	N/A	3 Prime UTR Variant
PDE3A transcript variant 1	NM_000921.5:c.*3651=	N/A	3 Prime UTR Variant
PDE3A transcript variant 3	NM_001378407.1:c.*3651=	N/A	3 Prime UTR Variant
PDE3A transcript variant 5	NM_001378409.1: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	A=	C	G	T
GRCh38.p14 chr 12	NC_000012.12:g.20683922=	NC_000012.12:g.20683922A>C	NC_000012.12:g.20683922A>G	NC_000012.12:g.20683922A>T
GRCh37.p13 chr 12	NC_000012.11:g.20836856=	NC_000012.11:g.20836856A>C	NC_000012.11:g.20836856A>G	NC_000012.11:g.20836856A>T
PDE3A RefSeqGene	NG_030033.1:g.319678=	NG_030033.1:g.319678A>C	NG_030033.1:g.319678A>G	NG_030033.1:g.319678A>T
PDE3A transcript variant 1	NM_000921.5:c.*3651=	NM_000921.5:c.*3651A>C	NM_000921.5:c.*3651A>G	NM_000921.5:c.*3651A>T
PDE3A transcript variant 1	NM_000921.4:c.*3651=	NM_000921.4:c.*3651A>C	NM_000921.4:c.*3651A>G	NM_000921.4:c.*3651A>T
PDE3A transcript variant 2	NM_001244683.2:c.*3651=	NM_001244683.2:c.*3651A>C	NM_001244683.2:c.*3651A>G	NM_001244683.2:c.*3651A>T
PDE3A transcript variant 2	NM_001244683.1:c.*3651=	NM_001244683.1:c.*3651A>C	NM_001244683.1:c.*3651A>G	NM_001244683.1:c.*3651A>T
PDE3A transcript variant 4	NM_001378408.1:c.*3805=	NM_001378408.1:c.*3805A>C	NM_001378408.1:c.*3805A>G	NM_001378408.1:c.*3805A>T
PDE3A transcript variant 3	NM_001378407.1:c.*3651=	NM_001378407.1:c.*3651A>C	NM_001378407.1:c.*3651A>G	NM_001378407.1:c.*3651A>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#.

103 SubSNP, 22 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	CGAP-GAI	ss16449	Sep 19, 2000 (52)
2	LEE	ss1516924	Oct 04, 2000 (86)
3	LEE	ss4392493	May 29, 2002 (106)
4	LEE	ss4409473	May 29, 2002 (106)
5	WI_SSAHASNP	ss12194759	Jul 11, 2003 (116)
6	SC_SNP	ss15510553	Feb 27, 2004 (120)
7	CGAP-GAI	ss16263700	Feb 27, 2004 (120)
8	SSAHASNP	ss20929848	Apr 05, 2004 (121)
9	ABI	ss38874083	Mar 14, 2006 (126)
10	HGSV	ss77676558	Dec 07, 2007 (129)
11	HGSV	ss85885138	Dec 15, 2007 (130)
12	BCMHGSC_JDW	ss89015265	Mar 24, 2008 (129)
13	HUMANGENOME_JCVI	ss97292091	Feb 05, 2009 (130)
14	KRIBB_YJKIM	ss104796382	Feb 05, 2009 (130)
15	BGI	ss106791818	Feb 05, 2009 (130)
16	HGSV	ss107791046	Feb 05, 2009 (130)
17	1000GENOMES	ss111604319	Jan 25, 2009 (130)
18	1000GENOMES	ss113259940	Jan 25, 2009 (130)
19	ILLUMINA-UK	ss118625402	Feb 14, 2009 (130)
20	ENSEMBL	ss133041061	Dec 01, 2009 (131)
21	ENSEMBL	ss137509643	Dec 01, 2009 (131)
22	GMI	ss157200469	Dec 01, 2009 (131)
23	ILLUMINA	ss159848928	Dec 01, 2009 (131)
24	COMPLETE_GENOMICS	ss167924377	Jul 04, 2010 (132)
25	ILLUMINA	ss168947462	Jul 04, 2010 (132)
26	COMPLETE_GENOMICS	ss169259012	Jul 04, 2010 (132)
27	BUSHMAN	ss203629601	Jul 04, 2010 (132)
28	BCM-HGSC-SUB	ss208244052	Jul 04, 2010 (132)
29	1000GENOMES	ss225642760	Jul 14, 2010 (132)
30	1000GENOMES	ss235852472	Jul 15, 2010 (132)
31	1000GENOMES	ss242425422	Jul 15, 2010 (132)
32	BL	ss254935328	May 09, 2011 (134)
33	GMI	ss281302441	May 04, 2012 (137)
34	PJP	ss291395886	May 09, 2011 (134)
35	ILLUMINA	ss479155795	Sep 08, 2015 (146)
36	ILLUMINA	ss532735213	Sep 08, 2015 (146)
37	TISHKOFF	ss563036760	Apr 25, 2013 (138)
38	SSMP	ss658571982	Apr 25, 2013 (138)
39	EVA-GONL	ss989312398	Aug 21, 2014 (142)
40	JMKIDD_LAB	ss1078301677	Aug 21, 2014 (142)
41	1000GENOMES	ss1344189214	Aug 21, 2014 (142)
42	DDI	ss1426866148	Apr 01, 2015 (144)
43	EVA_GENOME_DK	ss1576152869	Apr 01, 2015 (144)
44	EVA_DECODE	ss1598984933	Apr 01, 2015 (144)
45	EVA_UK10K_ALSPAC	ss1628158752	Apr 01, 2015 (144)
46	EVA_UK10K_TWINSUK	ss1671152785	Apr 01, 2015 (144)
47	HAMMER_LAB	ss1807151245	Sep 08, 2015 (146)
48	WEILL_CORNELL_DGM	ss1932676891	Feb 12, 2016 (147)
49	ILLUMINA	ss1946333372	Feb 12, 2016 (147)
50	ILLUMINA	ss1959419082	Feb 12, 2016 (147)
51	GENOMED	ss1967541242	Jul 19, 2016 (147)
52	JJLAB	ss2027085444	Sep 14, 2016 (149)
53	USC_VALOUEV	ss2155411096	Dec 20, 2016 (150)
54	HUMAN_LONGEVITY	ss2188342846	Dec 20, 2016 (150)
55	SYSTEMSBIOZJU	ss2628022072	Nov 08, 2017 (151)
56	ILLUMINA	ss2632934062	Nov 08, 2017 (151)
57	GRF	ss2699739050	Nov 08, 2017 (151)
58	GNOMAD	ss2908129577	Nov 08, 2017 (151)
59	SWEGEN	ss3009323084	Nov 08, 2017 (151)
60	ILLUMINA	ss3021412603	Nov 08, 2017 (151)
61	BIOINF_KMB_FNS_UNIBA	ss3027348800	Nov 08, 2017 (151)
62	CSHL	ss3349958321	Nov 08, 2017 (151)
63	ILLUMINA	ss3625617257	Oct 12, 2018 (152)
64	ILLUMINA	ss3626832448	Oct 12, 2018 (152)
65	ILLUMINA	ss3636178892	Oct 12, 2018 (152)
66	ILLUMINA	ss3637951140	Oct 12, 2018 (152)
67	ILLUMINA	ss3644586332	Oct 12, 2018 (152)
68	URBANLAB	ss3649784853	Oct 12, 2018 (152)
69	ILLUMINA	ss3651786667	Oct 12, 2018 (152)
70	EGCUT_WGS	ss3676638487	Jul 13, 2019 (153)
71	EVA_DECODE	ss3693251317	Jul 13, 2019 (153)
72	ILLUMINA	ss3725308905	Jul 13, 2019 (153)
73	ACPOP	ss3738832831	Jul 13, 2019 (153)
74	ILLUMINA	ss3744096207	Jul 13, 2019 (153)
75	EVA	ss3750225154	Jul 13, 2019 (153)
76	PAGE_CC	ss3771678855	Jul 13, 2019 (153)
77	PACBIO	ss3787165720	Jul 13, 2019 (153)
78	PACBIO	ss3792276552	Jul 13, 2019 (153)
79	PACBIO	ss3797159243	Jul 13, 2019 (153)
80	KHV_HUMAN_GENOMES	ss3815542532	Jul 13, 2019 (153)
81	EVA	ss3833011785	Apr 26, 2020 (154)
82	EVA	ss3840073553	Apr 26, 2020 (154)
83	EVA	ss3845557373	Apr 26, 2020 (154)
84	SGDP_PRJ	ss3877835799	Apr 26, 2020 (154)
85	KRGDB	ss3926367565	Apr 26, 2020 (154)
86	KOGIC	ss3971411309	Apr 26, 2020 (154)
87	EVA	ss3984663585	Apr 26, 2021 (155)
88	EVA	ss3985579478	Apr 26, 2021 (155)
89	TOPMED	ss4911070739	Apr 26, 2021 (155)
90	TOMMO_GENOMICS	ss5205376773	Apr 26, 2021 (155)
91	1000G_HIGH_COVERAGE	ss5290050142	Oct 13, 2022 (156)
92	EVA	ss5404359775	Oct 13, 2022 (156)
93	HUGCELL_USP	ss5484912335	Oct 13, 2022 (156)
94	EVA	ss5510617666	Oct 13, 2022 (156)
95	1000G_HIGH_COVERAGE	ss5587099070	Oct 13, 2022 (156)
96	SANFORD_IMAGENETICS	ss5652730746	Oct 13, 2022 (156)
97	TOMMO_GENOMICS	ss5754267967	Oct 13, 2022 (156)
98	YY_MCH	ss5813074296	Oct 13, 2022 (156)
99	EVA	ss5837684646	Oct 13, 2022 (156)
100	EVA	ss5847662686	Oct 13, 2022 (156)
101	EVA	ss5850289592	Oct 13, 2022 (156)
102	EVA	ss5903557802	Oct 13, 2022 (156)
103	EVA	ss5944081743	Oct 13, 2022 (156)
104	1000Genomes	NC_000012.11 - 20836856	Oct 12, 2018 (152)
105	1000Genomes_30x	NC_000012.12 - 20683922	Oct 13, 2022 (156)
106	The Avon Longitudinal Study of Parents and Children	NC_000012.11 - 20836856	Oct 12, 2018 (152)
107	Genetic variation in the Estonian population	NC_000012.11 - 20836856	Oct 12, 2018 (152)
108	The Danish reference pan genome	NC_000012.11 - 20836856	Apr 26, 2020 (154)
109	gnomAD - Genomes	NC_000012.12 - 20683922	Apr 26, 2021 (155)
110	Genome of the Netherlands Release 5	NC_000012.11 - 20836856	Apr 26, 2020 (154)
111	KOREAN population from KRGDB	NC_000012.11 - 20836856	Apr 26, 2020 (154)
112	Korean Genome Project	NC_000012.12 - 20683922	Apr 26, 2020 (154)
113	Northern Sweden	NC_000012.11 - 20836856	Jul 13, 2019 (153)
114	The PAGE Study	NC_000012.12 - 20683922	Jul 13, 2019 (153)
115	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000012.11 - 20836856	Apr 26, 2021 (155)
116	CNV burdens in cranial meningiomas	NC_000012.11 - 20836856	Apr 26, 2021 (155)
117	Qatari	NC_000012.11 - 20836856	Apr 26, 2020 (154)
118	SGDP_PRJ	NC_000012.11 - 20836856	Apr 26, 2020 (154)
119	Siberian	NC_000012.11 - 20836856	Apr 26, 2020 (154)
120	8.3KJPN	NC_000012.11 - 20836856	Apr 26, 2021 (155)
121	14KJPN	NC_000012.12 - 20683922	Oct 13, 2022 (156)
122	TopMed	NC_000012.12 - 20683922	Apr 26, 2021 (155)
123	UK 10K study - Twins	NC_000012.11 - 20836856	Oct 12, 2018 (152)
124	A Vietnamese Genetic Variation Database	NC_000012.11 - 20836856	Jul 13, 2019 (153)
125	ALFA	NC_000012.12 - 20683922	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)
rs3168547	Jul 03, 2002 (106)
rs59360778	May 25, 2008 (130)
rs117088200	Aug 16, 2010 (132)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss203629601	NC_000012.10:20728122:A:C	NC_000012.12:20683921:A:C	(self)
33544959, ss3926367565	NC_000012.11:20836855:A:C	NC_000012.12:20683921:A:C	(self)
ss77676558, ss85885138	NC_000012.9:20728122:A:G	NC_000012.12:20683921:A:G	(self)
ss89015265, ss111604319, ss113259940, ss118625402, ss167924377, ss169259012, ss203629601, ss208244052, ss254935328, ss281302441, ss291395886, ss1598984933	NC_000012.10:20728122:A:G	NC_000012.12:20683921:A:G	(self)
56907221, 31598410, 22376735, 2873463, 14098909, 33544959, 12117696, 805405, 213077, 14718821, 29852779, 7927450, 63346080, 31598410, 7010863, ss225642760, ss235852472, ss242425422, ss479155795, ss532735213, ss563036760, ss658571982, ss989312398, ss1078301677, ss1344189214, ss1426866148, ss1576152869, ss1628158752, ss1671152785, ss1807151245, ss1932676891, ss1946333372, ss1959419082, ss1967541242, ss2027085444, ss2155411096, ss2628022072, ss2632934062, ss2699739050, ss2908129577, ss3009323084, ss3021412603, ss3349958321, ss3625617257, ss3626832448, ss3636178892, ss3637951140, ss3644586332, ss3651786667, ss3676638487, ss3738832831, ss3744096207, ss3750225154, ss3787165720, ss3792276552, ss3797159243, ss3833011785, ss3840073553, ss3877835799, ss3926367565, ss3984663585, ss3985579478, ss5205376773, ss5404359775, ss5510617666, ss5652730746, ss5837684646, ss5847662686, ss5944081743	NC_000012.11:20836855:A:G	NC_000012.12:20683921:A:G	(self)
74625005, 401266573, 27789310, 900324, 88105071, 126616396, 6092468772, ss2188342846, ss3027348800, ss3649784853, ss3693251317, ss3725308905, ss3771678855, ss3815542532, ss3845557373, ss3971411309, ss4911070739, ss5290050142, ss5484912335, ss5587099070, ss5754267967, ss5813074296, ss5850289592, ss5903557802	NC_000012.12:20683921:A:G	NC_000012.12:20683921:A:G	(self)
ss12194759	NT_009714.15:13595829:A:G	NC_000012.12:20683921:A:G	(self)
ss15510553, ss20929848	NT_009714.16:13595829:A:G	NC_000012.12:20683921:A:G	(self)
ss16449, ss1516924, ss4392493, ss4409473, ss16263700, ss38874083, ss97292091, ss104796382, ss106791818, ss107791046, ss133041061, ss137509643, ss157200469, ss159848928, ss168947462	NT_009714.17:13596979:A:G	NC_000012.12:20683921:A:G	(self)
ss203629601	NC_000012.10:20728122:A:T	NC_000012.12:20683921:A:T	(self)
33544959, ss3926367565	NC_000012.11:20836855:A:T	NC_000012.12:20683921:A:T	(self)
6092468772	NC_000012.12:20683921:A:T	NC_000012.12:20683921:A: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 rs14083

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

rs14083