Name: rs4596036
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.

rs4596036

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr20:48642075 (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: G>A
Variation Type: SNV Single Nucleotide Variation
Frequency: A=0.261351 (69177/264690, TOPMED)
A=0.252911 (35442/140136, GnomAD)
A=0.27042 (19509/72142, ALFA) (+ 19 more)
A=0.32743 (9252/28256, 14KJPN)
A=0.32924 (5518/16760, 8.3KJPN)
A=0.2890 (1851/6404, 1000G_30x)
A=0.2945 (1475/5008, 1000G)
A=0.2049 (918/4480, Estonian)
A=0.2543 (980/3854, ALSPAC)
A=0.2767 (1026/3708, TWINSUK)
A=0.2625 (769/2930, KOREAN)
A=0.3191 (665/2084, HGDP_Stanford)
A=0.2560 (469/1832, Korea1K)
A=0.248 (248/998, GoNL)
A=0.222 (133/600, NorthernSweden)
A=0.199 (106/534, MGP)
G=0.386 (112/290, SGDP_PRJ)
A=0.444 (96/216, Qatari)
A=0.219 (46/210, Vietnamese)
A=0.49 (34/70, Ancient Sardinia)
A=0.35 (14/40, GENOME_DK)
G=0.38 (12/32, Siberian)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: PREX1 : 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	72142	G=0.72958	A=0.27042
European	Sub	59468	G=0.73635	A=0.26365
African	Sub	4540	G=0.7815	A=0.2185
African Others	Sub	170	G=0.776	A=0.224
African American	Sub	4370	G=0.7817	A=0.2183
Asian	Sub	190	G=0.732	A=0.268
East Asian	Sub	148	G=0.736	A=0.264
Other Asian	Sub	42	G=0.71	A=0.29
Latin American 1	Sub	254	G=0.713	A=0.287
Latin American 2	Sub	1232	G=0.6339	A=0.3661
South Asian	Sub	4956	G=0.6316	A=0.3684
Other	Sub	1502	G=0.7091	A=0.2909

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	G=0.738649	A=0.261351
gnomAD - Genomes	Global	Study-wide	140136	G=0.747089	A=0.252911
gnomAD - Genomes	European	Sub	75878	G=0.74340	A=0.25660
gnomAD - Genomes	African	Sub	42034	G=0.78915	A=0.21085
gnomAD - Genomes	American	Sub	13630	G=0.66244	A=0.33756
gnomAD - Genomes	Ashkenazi Jewish	Sub	3324	G=0.6673	A=0.3327
gnomAD - Genomes	East Asian	Sub	3120	G=0.7429	A=0.2571
gnomAD - Genomes	Other	Sub	2150	G=0.7209	A=0.2791
Allele Frequency Aggregator	Total	Global	72142	G=0.72958	A=0.27042
Allele Frequency Aggregator	European	Sub	59468	G=0.73635	A=0.26365
Allele Frequency Aggregator	South Asian	Sub	4956	G=0.6316	A=0.3684
Allele Frequency Aggregator	African	Sub	4540	G=0.7815	A=0.2185
Allele Frequency Aggregator	Other	Sub	1502	G=0.7091	A=0.2909
Allele Frequency Aggregator	Latin American 2	Sub	1232	G=0.6339	A=0.3661
Allele Frequency Aggregator	Latin American 1	Sub	254	G=0.713	A=0.287
Allele Frequency Aggregator	Asian	Sub	190	G=0.732	A=0.268
14KJPN	JAPANESE	Study-wide	28256	G=0.67257	A=0.32743
8.3KJPN	JAPANESE	Study-wide	16760	G=0.67076	A=0.32924
1000Genomes_30x	Global	Study-wide	6404	G=0.7110	A=0.2890
1000Genomes_30x	African	Sub	1786	G=0.8080	A=0.1920
1000Genomes_30x	Europe	Sub	1266	G=0.7354	A=0.2646
1000Genomes_30x	South Asian	Sub	1202	G=0.5890	A=0.4110
1000Genomes_30x	East Asian	Sub	1170	G=0.7120	A=0.2880
1000Genomes_30x	American	Sub	980	G=0.651	A=0.349
1000Genomes	Global	Study-wide	5008	G=0.7055	A=0.2945
1000Genomes	African	Sub	1322	G=0.7980	A=0.2020
1000Genomes	East Asian	Sub	1008	G=0.7113	A=0.2887
1000Genomes	Europe	Sub	1006	G=0.7386	A=0.2614
1000Genomes	South Asian	Sub	978	G=0.578	A=0.422
1000Genomes	American	Sub	694	G=0.653	A=0.347
Genetic variation in the Estonian population	Estonian	Study-wide	4480	G=0.7951	A=0.2049
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	G=0.7457	A=0.2543
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	G=0.7233	A=0.2767
KOREAN population from KRGDB	KOREAN	Study-wide	2930	G=0.7375	A=0.2625
HGDP-CEPH-db Supplement 1	Global	Study-wide	2084	G=0.6809	A=0.3191
HGDP-CEPH-db Supplement 1	Est_Asia	Sub	470	G=0.764	A=0.236
HGDP-CEPH-db Supplement 1	Central_South_Asia	Sub	414	G=0.580	A=0.420
HGDP-CEPH-db Supplement 1	Middle_Est	Sub	350	G=0.637	A=0.363
HGDP-CEPH-db Supplement 1	Europe	Sub	320	G=0.744	A=0.256
HGDP-CEPH-db Supplement 1	Africa	Sub	242	G=0.781	A=0.219
HGDP-CEPH-db Supplement 1	America	Sub	216	G=0.588	A=0.412
HGDP-CEPH-db Supplement 1	Oceania	Sub	72	G=0.60	A=0.40
Korean Genome Project	KOREAN	Study-wide	1832	G=0.7440	A=0.2560
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	G=0.752	A=0.248
Northern Sweden	ACPOP	Study-wide	600	G=0.778	A=0.222
Medical Genome Project healthy controls from Spanish population	Spanish controls	Study-wide	534	G=0.801	A=0.199
SGDP_PRJ	Global	Study-wide	290	G=0.386	A=0.614
Qatari	Global	Study-wide	216	G=0.556	A=0.444
A Vietnamese Genetic Variation Database	Global	Study-wide	210	G=0.781	A=0.219
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	70	G=0.51	A=0.49
The Danish reference pan genome	Danish	Study-wide	40	G=0.65	A=0.35
Siberian	Global	Study-wide	32	G=0.38	A=0.62

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 20	NC_000020.11:g.48642075G>A
GRCh37.p13 chr 20	NC_000020.10:g.47258613G>A

Gene: PREX1, phosphatidylinositol-3,4,5-trisphosphate dependent Rac exchange factor 1 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
PREX1 transcript	NM_020820.4:c.3775+93C>T	N/A	Intron Variant
PREX1 transcript variant X4	XM_011528934.2:c.2575+93C… XM_011528934.2:c.2575+93C>T	N/A	Intron Variant
PREX1 transcript variant X1	XM_047440331.1:c.3250+93C… XM_047440331.1:c.3250+93C>T	N/A	Intron Variant
PREX1 transcript variant X2	XM_047440332.1:c.3250+93C… XM_047440332.1:c.3250+93C>T	N/A	Intron Variant
PREX1 transcript variant X3	XM_047440333.1:c.3250+93C… XM_047440333.1:c.3250+93C>T	N/A	Intron Variant
PREX1 transcript variant X5	XM_047440334.1:c.1912+93C… XM_047440334.1:c.1912+93C>T	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	G=	A
GRCh38.p14 chr 20	NC_000020.11:g.48642075=	NC_000020.11:g.48642075G>A
GRCh37.p13 chr 20	NC_000020.10:g.47258613=	NC_000020.10:g.47258613G>A
PREX1 transcript	NM_020820.3:c.3775+93=	NM_020820.3:c.3775+93C>T
PREX1 transcript	NM_020820.4:c.3775+93=	NM_020820.4:c.3775+93C>T
PREX1 transcript variant X1	XM_005260471.1:c.1666+93=	XM_005260471.1:c.1666+93C>T
PREX1 transcript variant X4	XM_011528934.2:c.2575+93=	XM_011528934.2:c.2575+93C>T
PREX1 transcript variant X1	XM_047440331.1:c.3250+93=	XM_047440331.1:c.3250+93C>T
PREX1 transcript variant X2	XM_047440332.1:c.3250+93=	XM_047440332.1:c.3250+93C>T
PREX1 transcript variant X3	XM_047440333.1:c.3250+93=	XM_047440333.1:c.3250+93C>T
PREX1 transcript variant X5	XM_047440334.1:c.1912+93=	XM_047440334.1:c.1912+93C>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#.

101 SubSNP, 22 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	SC_JCM	ss6225780	Feb 20, 2003 (111)
2	SC_SNP	ss8379247	Apr 21, 2003 (114)
3	ILLUMINA	ss65760463	Oct 16, 2006 (127)
4	ILLUMINA	ss66651254	Dec 02, 2006 (127)
5	ILLUMINA	ss67348801	Dec 02, 2006 (127)
6	ILLUMINA	ss67740958	Dec 02, 2006 (127)
7	CSHL-HAPMAP	ss68413479	Jan 12, 2007 (127)
8	ILLUMINA	ss70810919	May 23, 2008 (130)
9	ILLUMINA	ss71391122	May 18, 2007 (127)
10	ILLUMINA	ss75493916	Dec 06, 2007 (129)
11	SI_EXO	ss76887747	Dec 06, 2007 (129)
12	ILLUMINA	ss79186416	Dec 14, 2007 (130)
13	HGSV	ss80236815	Dec 14, 2007 (130)
14	KRIBB_YJKIM	ss84296151	Dec 14, 2007 (130)
15	BGI	ss103764666	Dec 01, 2009 (131)
16	1000GENOMES	ss112056473	Jan 25, 2009 (130)
17	1000GENOMES	ss113410339	Jan 25, 2009 (130)
18	ILLUMINA-UK	ss117565494	Feb 14, 2009 (130)
19	ILLUMINA	ss122335778	Dec 01, 2009 (131)
20	ILLUMINA	ss154301794	Dec 01, 2009 (131)
21	ILLUMINA	ss159478634	Dec 01, 2009 (131)
22	COMPLETE_GENOMICS	ss169773923	Jul 04, 2010 (132)
23	ILLUMINA	ss171832435	Jul 04, 2010 (132)
24	ILLUMINA	ss173758602	Jul 04, 2010 (132)
25	BUSHMAN	ss203907430	Jul 04, 2010 (132)
26	1000GENOMES	ss228384818	Jul 14, 2010 (132)
27	1000GENOMES	ss237853758	Jul 15, 2010 (132)
28	1000GENOMES	ss244021071	Jul 15, 2010 (132)
29	BL	ss255683364	May 09, 2011 (134)
30	GMI	ss283403049	May 04, 2012 (137)
31	ILLUMINA	ss537248453	Sep 08, 2015 (146)
32	TISHKOFF	ss566289314	Apr 25, 2013 (138)
33	SSMP	ss662169952	Apr 25, 2013 (138)
34	ILLUMINA	ss825516934	Jul 19, 2016 (147)
35	ILLUMINA	ss832990082	Jul 13, 2019 (153)
36	EVA-GONL	ss994785725	Aug 21, 2014 (142)
37	JMKIDD_LAB	ss1082251060	Aug 21, 2014 (142)
38	1000GENOMES	ss1365027721	Aug 21, 2014 (142)
39	DDI	ss1429071712	Apr 01, 2015 (144)
40	EVA_GENOME_DK	ss1579530020	Apr 01, 2015 (144)
41	EVA_UK10K_ALSPAC	ss1638914743	Apr 01, 2015 (144)
42	EVA_UK10K_TWINSUK	ss1681908776	Apr 01, 2015 (144)
43	EVA_DECODE	ss1698846461	Apr 01, 2015 (144)
44	EVA_MGP	ss1711543424	Apr 01, 2015 (144)
45	EVA_SVP	ss1713698927	Apr 01, 2015 (144)
46	HAMMER_LAB	ss1809530010	Sep 08, 2015 (146)
47	WEILL_CORNELL_DGM	ss1938301144	Feb 12, 2016 (147)
48	GENOMED	ss1969145883	Jul 19, 2016 (147)
49	JJLAB	ss2029930099	Sep 14, 2016 (149)
50	USC_VALOUEV	ss2158499502	Dec 20, 2016 (150)
51	HUMAN_LONGEVITY	ss2243281493	Dec 20, 2016 (150)
52	SYSTEMSBIOZJU	ss2629459199	Nov 08, 2017 (151)
53	ILLUMINA	ss2635106364	Nov 08, 2017 (151)
54	GRF	ss2704193731	Nov 08, 2017 (151)
55	GNOMAD	ss2968145237	Nov 08, 2017 (151)
56	SWEGEN	ss3018285478	Nov 08, 2017 (151)
57	BIOINF_KMB_FNS_UNIBA	ss3028797966	Nov 08, 2017 (151)
58	CSHL	ss3352539213	Nov 08, 2017 (151)
59	ILLUMINA	ss3628407026	Oct 12, 2018 (152)
60	ILLUMINA	ss3638349903	Oct 12, 2018 (152)
61	ILLUMINA	ss3639178236	Oct 12, 2018 (152)
62	ILLUMINA	ss3639603504	Oct 12, 2018 (152)
63	ILLUMINA	ss3643312342	Oct 12, 2018 (152)
64	OMUKHERJEE_ADBS	ss3646550651	Oct 12, 2018 (152)
65	EGCUT_WGS	ss3684969441	Jul 13, 2019 (153)
66	EVA_DECODE	ss3707072827	Jul 13, 2019 (153)
67	ACPOP	ss3743447226	Jul 13, 2019 (153)
68	EVA	ss3758723082	Jul 13, 2019 (153)
69	KHV_HUMAN_GENOMES	ss3821881959	Jul 13, 2019 (153)
70	EVA	ss3835703360	Apr 27, 2020 (154)
71	EVA	ss3841475686	Apr 27, 2020 (154)
72	EVA	ss3846988727	Apr 27, 2020 (154)
73	HGDP	ss3847669460	Apr 27, 2020 (154)
74	SGDP_PRJ	ss3889235426	Apr 27, 2020 (154)
75	KRGDB	ss3939538589	Apr 27, 2020 (154)
76	KOGIC	ss3982412966	Apr 27, 2020 (154)
77	FSA-LAB	ss3984218414	Apr 27, 2021 (155)
78	EVA	ss3985883467	Apr 27, 2021 (155)
79	EVA	ss3986834117	Apr 27, 2021 (155)
80	EVA	ss4017851532	Apr 27, 2021 (155)
81	TOPMED	ss5090835718	Apr 27, 2021 (155)
82	TOMMO_GENOMICS	ss5229941751	Apr 27, 2021 (155)
83	EVA	ss5237252350	Apr 27, 2021 (155)
84	1000G_HIGH_COVERAGE	ss5309025943	Oct 13, 2022 (156)
85	EVA	ss5437820789	Oct 13, 2022 (156)
86	HUGCELL_USP	ss5501281593	Oct 13, 2022 (156)
87	EVA	ss5512235286	Oct 13, 2022 (156)
88	1000G_HIGH_COVERAGE	ss5615593860	Oct 13, 2022 (156)
89	EVA	ss5623981258	Oct 13, 2022 (156)
90	EVA	ss5624114513	Oct 13, 2022 (156)
91	SANFORD_IMAGENETICS	ss5663339187	Oct 13, 2022 (156)
92	TOMMO_GENOMICS	ss5789835733	Oct 13, 2022 (156)
93	EVA	ss5800230228	Oct 13, 2022 (156)
94	YY_MCH	ss5818100807	Oct 13, 2022 (156)
95	EVA	ss5845780682	Oct 13, 2022 (156)
96	EVA	ss5848550258	Oct 13, 2022 (156)
97	EVA	ss5853167734	Oct 13, 2022 (156)
98	EVA	ss5923688201	Oct 13, 2022 (156)
99	EVA	ss5936577512	Oct 13, 2022 (156)
100	EVA	ss5958262360	Oct 13, 2022 (156)
101	EVA	ss5981091626	Oct 13, 2022 (156)
102	1000Genomes	NC_000020.10 - 47258613	Oct 12, 2018 (152)
103	1000Genomes_30x	NC_000020.11 - 48642075	Oct 13, 2022 (156)
104	The Avon Longitudinal Study of Parents and Children	NC_000020.10 - 47258613	Oct 12, 2018 (152)
105	Genetic variation in the Estonian population	NC_000020.10 - 47258613	Oct 12, 2018 (152)
106	The Danish reference pan genome	NC_000020.10 - 47258613	Apr 27, 2020 (154)
107	gnomAD - Genomes	NC_000020.11 - 48642075	Apr 27, 2021 (155)
108	Genome of the Netherlands Release 5	NC_000020.10 - 47258613	Apr 27, 2020 (154)
109	HGDP-CEPH-db Supplement 1	NC_000020.9 - 46692020	Apr 27, 2020 (154)
110	KOREAN population from KRGDB	NC_000020.10 - 47258613	Apr 27, 2020 (154)
111	Korean Genome Project	NC_000020.11 - 48642075	Apr 27, 2020 (154)
112	Medical Genome Project healthy controls from Spanish population	NC_000020.10 - 47258613	Apr 27, 2020 (154)
113	Northern Sweden	NC_000020.10 - 47258613	Jul 13, 2019 (153)
114	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000020.10 - 47258613	Apr 27, 2021 (155)
115	Qatari	NC_000020.10 - 47258613	Apr 27, 2020 (154)
116	SGDP_PRJ	NC_000020.10 - 47258613	Apr 27, 2020 (154)
117	Siberian	NC_000020.10 - 47258613	Apr 27, 2020 (154)
118	8.3KJPN	NC_000020.10 - 47258613	Apr 27, 2021 (155)
119	14KJPN	NC_000020.11 - 48642075	Oct 13, 2022 (156)
120	TopMed	NC_000020.11 - 48642075	Apr 27, 2021 (155)
121	UK 10K study - Twins	NC_000020.10 - 47258613	Oct 12, 2018 (152)
122	A Vietnamese Genetic Variation Database	NC_000020.10 - 47258613	Jul 13, 2019 (153)
123	ALFA	NC_000020.11 - 48642075	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)
rs56757285	May 23, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
347352, ss80236815, ss112056473, ss113410339, ss117565494, ss169773923, ss203907430, ss255683364, ss283403049, ss825516934, ss1698846461, ss1713698927, ss2635106364, ss3639178236, ss3639603504, ss3643312342, ss3847669460	NC_000020.9:46692019:G:A	NC_000020.11:48642074:G:A	(self)
78499794, 43455440, 30707689, 5694959, 19356835, 46715983, 659184, 16732091, 1109394, 20343066, 41252406, 11015856, 87911058, 43455440, 9586844, ss228384818, ss237853758, ss244021071, ss537248453, ss566289314, ss662169952, ss832990082, ss994785725, ss1082251060, ss1365027721, ss1429071712, ss1579530020, ss1638914743, ss1681908776, ss1711543424, ss1809530010, ss1938301144, ss1969145883, ss2029930099, ss2158499502, ss2629459199, ss2704193731, ss2968145237, ss3018285478, ss3352539213, ss3628407026, ss3638349903, ss3646550651, ss3684969441, ss3743447226, ss3758723082, ss3835703360, ss3841475686, ss3889235426, ss3939538589, ss3984218414, ss3985883467, ss3986834117, ss4017851532, ss5229941751, ss5437820789, ss5512235286, ss5623981258, ss5624114513, ss5663339187, ss5800230228, ss5845780682, ss5848550258, ss5936577512, ss5958262360, ss5981091626	NC_000020.10:47258612:G:A	NC_000020.11:48642074:G:A	(self)
103119795, 553707258, 38790967, 123672837, 365944663, 4559821711, ss2243281493, ss3028797966, ss3707072827, ss3821881959, ss3846988727, ss3982412966, ss5090835718, ss5237252350, ss5309025943, ss5501281593, ss5615593860, ss5789835733, ss5818100807, ss5853167734, ss5923688201	NC_000020.11:48642074:G:A	NC_000020.11:48642074:G:A	(self)
ss76887747	NT_011362.9:12311520:G:A	NC_000020.11:48642074:G:A	(self)
ss6225780, ss8379247, ss65760463, ss66651254, ss67348801, ss67740958, ss68413479, ss70810919, ss71391122, ss75493916, ss79186416, ss84296151, ss103764666, ss122335778, ss154301794, ss159478634, ss171832435, ss173758602	NT_011362.10:17454704:G:A	NC_000020.11:48642074:G: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 rs4596036

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.

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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs4596036