Name: rs3734464
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.

rs3734464

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr6:161348803 (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>C
Variation Type: SNV Single Nucleotide Variation
Frequency: C=0.077600 (20540/264690, TOPMED)
C=0.094560 (19580/207064, ALFA)
C=0.083122 (11658/140252, GnomAD) (+ 20 more)
C=0.02099 (593/28258, 14KJPN)
C=0.02166 (363/16760, 8.3KJPN)
C=0.0572 (366/6404, 1000G_30x)
C=0.0577 (289/5008, 1000G)
C=0.1129 (506/4480, Estonian)
C=0.0983 (379/3854, ALSPAC)
C=0.0952 (353/3708, TWINSUK)
C=0.0171 (50/2922, KOREAN)
C=0.0801 (167/2084, HGDP_Stanford)
C=0.0576 (109/1892, HapMap)
C=0.0169 (31/1832, Korea1K)
C=0.127 (127/998, GoNL)
C=0.061 (38/626, Chileans)
C=0.130 (78/600, NorthernSweden)
C=0.056 (12/216, Qatari)
T=0.39 (33/84, SGDP_PRJ)
C=0.08 (6/78, Ancient Sardinia)
C=0.05 (2/40, GENOME_DK)
T=0.5 (4/8, Siberian)
C=0.5 (4/8, Siberian)

Clinical Significance: Reported in ClinVar
Gene : Consequence: PRKN : 3 Prime UTR Variant
Publications: 1 citation
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	207064	T=0.905440	C=0.094560
European	Sub	176156	T=0.900963	C=0.099037
African	Sub	7768	T=0.9377	C=0.0623
African Others	Sub	276	T=0.946	C=0.054
African American	Sub	7492	T=0.9374	C=0.0626
Asian	Sub	750	T=0.992	C=0.008
East Asian	Sub	572	T=0.991	C=0.009
Other Asian	Sub	178	T=0.994	C=0.006
Latin American 1	Sub	988	T=0.924	C=0.076
Latin American 2	Sub	9016	T=0.9419	C=0.0581
South Asian	Sub	5052	T=0.9210	C=0.0790
Other	Sub	7334	T=0.9119	C=0.0881

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").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
TopMed	Global	Study-wide	264690	T=0.922400	C=0.077600
Allele Frequency Aggregator	Total	Global	207064	T=0.905440	C=0.094560
Allele Frequency Aggregator	European	Sub	176156	T=0.900963	C=0.099037
Allele Frequency Aggregator	Latin American 2	Sub	9016	T=0.9419	C=0.0581
Allele Frequency Aggregator	African	Sub	7768	T=0.9377	C=0.0623
Allele Frequency Aggregator	Other	Sub	7334	T=0.9119	C=0.0881
Allele Frequency Aggregator	South Asian	Sub	5052	T=0.9210	C=0.0790
Allele Frequency Aggregator	Latin American 1	Sub	988	T=0.924	C=0.076
Allele Frequency Aggregator	Asian	Sub	750	T=0.992	C=0.008
gnomAD - Genomes	Global	Study-wide	140252	T=0.916878	C=0.083122
gnomAD - Genomes	European	Sub	75930	T=0.90137	C=0.09863
gnomAD - Genomes	African	Sub	42050	T=0.93943	C=0.06057
gnomAD - Genomes	American	Sub	13662	T=0.92856	C=0.07144
gnomAD - Genomes	Ashkenazi Jewish	Sub	3322	T=0.8694	C=0.1306
gnomAD - Genomes	East Asian	Sub	3134	T=0.9914	C=0.0086
gnomAD - Genomes	Other	Sub	2154	T=0.9141	C=0.0859
14KJPN	JAPANESE	Study-wide	28258	T=0.97901	C=0.02099
8.3KJPN	JAPANESE	Study-wide	16760	T=0.97834	C=0.02166
1000Genomes_30x	Global	Study-wide	6404	T=0.9428	C=0.0572
1000Genomes_30x	African	Sub	1786	T=0.9535	C=0.0465
1000Genomes_30x	Europe	Sub	1266	T=0.9021	C=0.0979
1000Genomes_30x	South Asian	Sub	1202	T=0.9359	C=0.0641
1000Genomes_30x	East Asian	Sub	1170	T=0.9838	C=0.0162
1000Genomes_30x	American	Sub	980	T=0.936	C=0.064
1000Genomes	Global	Study-wide	5008	T=0.9423	C=0.0577
1000Genomes	African	Sub	1322	T=0.9523	C=0.0477
1000Genomes	East Asian	Sub	1008	T=0.9841	C=0.0159
1000Genomes	Europe	Sub	1006	T=0.8986	C=0.1014
1000Genomes	South Asian	Sub	978	T=0.934	C=0.066
1000Genomes	American	Sub	694	T=0.938	C=0.062
Genetic variation in the Estonian population	Estonian	Study-wide	4480	T=0.8871	C=0.1129
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	T=0.9017	C=0.0983
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	T=0.9048	C=0.0952
KOREAN population from KRGDB	KOREAN	Study-wide	2922	T=0.9829	C=0.0171
HGDP-CEPH-db Supplement 1	Global	Study-wide	2084	T=0.9199	C=0.0801
HGDP-CEPH-db Supplement 1	Est_Asia	Sub	470	T=0.979	C=0.021
HGDP-CEPH-db Supplement 1	Central_South_Asia	Sub	414	T=0.889	C=0.111
HGDP-CEPH-db Supplement 1	Middle_Est	Sub	350	T=0.900	C=0.100
HGDP-CEPH-db Supplement 1	Europe	Sub	320	T=0.900	C=0.100
HGDP-CEPH-db Supplement 1	Africa	Sub	242	T=0.909	C=0.091
HGDP-CEPH-db Supplement 1	America	Sub	216	T=0.986	C=0.014
HGDP-CEPH-db Supplement 1	Oceania	Sub	72	T=0.74	C=0.26
HapMap	Global	Study-wide	1892	T=0.9424	C=0.0576
HapMap	American	Sub	770	T=0.960	C=0.040
HapMap	African	Sub	692	T=0.921	C=0.079
HapMap	Asian	Sub	254	T=0.984	C=0.016
HapMap	Europe	Sub	176	T=0.892	C=0.108
Korean Genome Project	KOREAN	Study-wide	1832	T=0.9831	C=0.0169
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	T=0.873	C=0.127
Chileans	Chilean	Study-wide	626	T=0.939	C=0.061
Northern Sweden	ACPOP	Study-wide	600	T=0.870	C=0.130
Qatari	Global	Study-wide	216	T=0.944	C=0.056
SGDP_PRJ	Global	Study-wide	84	T=0.39	C=0.61
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	78	T=0.92	C=0.08
The Danish reference pan genome	Danish	Study-wide	40	T=0.95	C=0.05
Siberian	Global	Study-wide	8	T=0.5	C=0.5

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 6	NC_000006.12:g.161348803T>C
GRCh37.p13 chr 6	NC_000006.11:g.161769835T>C
PRKN RefSeqGene	NG_008289.2:g.1384000A>G

Gene: PRKN, parkin RBR E3 ubiquitin protein ligase (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
PRKN transcript variant 1	NM_004562.3:c.*1296=	N/A	3 Prime UTR Variant
PRKN transcript variant 2	NM_013987.3:c.*1296=	N/A	3 Prime UTR Variant
PRKN transcript variant 3	NM_013988.3:c.*1296=	N/A	3 Prime UTR Variant
PRKN transcript variant X1	XM_017010908.2:c.*1296=	N/A	3 Prime UTR Variant
PRKN transcript variant X2	XM_011535863.2:c.*1296=	N/A	3 Prime UTR Variant
PRKN transcript variant X3	XM_024446449.2:c.*1296=	N/A	3 Prime UTR 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.

Allele: C (allele ID: 302100 )

ClinVar Accession	Disease Names	Clinical Significance
RCV000376877.3	Autosomal recessive juvenile Parkinson disease 2	Benign

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=	C
GRCh38.p14 chr 6	NC_000006.12:g.161348803=	NC_000006.12:g.161348803T>C
GRCh37.p13 chr 6	NC_000006.11:g.161769835=	NC_000006.11:g.161769835T>C
PRKN RefSeqGene	NG_008289.2:g.1384000=	NG_008289.2:g.1384000A>G
PRKN transcript variant 1	NM_004562.3:c.*1296=	NM_004562.3:c.*1296A>G
PRKN transcript variant 1	NM_004562.2:c.*1296=	NM_004562.2:c.*1296A>G
PRKN transcript variant 2	NM_013987.3:c.*1296=	NM_013987.3:c.*1296A>G
PRKN transcript variant 2	NM_013987.2:c.*1296=	NM_013987.2:c.*1296A>G
PRKN transcript variant 3	NM_013988.3:c.*1296=	NM_013988.3:c.*1296A>G
PRKN transcript variant 3	NM_013988.2:c.*1296=	NM_013988.2:c.*1296A>G
PRKN transcript variant X1	XM_017010908.2:c.*1296=	XM_017010908.2:c.*1296A>G
PRKN transcript variant X1	XM_017010908.1:c.*1296=	XM_017010908.1:c.*1296A>G
PRKN transcript variant X2	XM_011535863.2:c.*1296=	XM_011535863.2:c.*1296A>G
PRKN transcript variant X2	XM_011535863.1:c.*1296=	XM_011535863.1:c.*1296A>G
PRKN transcript variant X3	XM_024446449.2:c.*1296=	XM_024446449.2:c.*1296A>G
PRKN transcript variant X3	XM_024446449.1:c.*1296=	XM_024446449.1:c.*1296A>G

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#.

108 SubSNP, 22 Frequency, 1 ClinVar submissions

No	Submitter	Submission ID	Date (Build)
1	YUSUKE	ss4920461	Aug 28, 2002 (107)
2	PERLEGEN	ss24470215	Sep 20, 2004 (123)
3	AFFY	ss66430441	Nov 29, 2006 (127)
4	ILLUMINA	ss66746334	Nov 29, 2006 (127)
5	ILLUMINA	ss67297745	Nov 29, 2006 (127)
6	ILLUMINA	ss67702284	Nov 29, 2006 (127)
7	PERLEGEN	ss68998891	May 16, 2007 (127)
8	ILLUMINA	ss70776373	May 26, 2008 (130)
9	ILLUMINA	ss71352451	May 16, 2007 (127)
10	ILLUMINA	ss75696494	Dec 06, 2007 (129)
11	AFFY	ss76202864	Dec 06, 2007 (129)
12	ILLUMINA	ss79163378	Dec 15, 2007 (130)
13	KRIBB_YJKIM	ss84159737	Dec 15, 2007 (130)
14	BCMHGSC_JDW	ss93595443	Mar 24, 2008 (129)
15	SHGC	ss99307790	Feb 06, 2009 (130)
16	ILLUMINA	ss122200086	Dec 01, 2009 (131)
17	ENSEMBL	ss142474102	Dec 01, 2009 (131)
18	ILLUMINA	ss154263471	Dec 01, 2009 (131)
19	ILLUMINA	ss159440336	Dec 01, 2009 (131)
20	ILLUMINA	ss160632621	Dec 01, 2009 (131)
21	COMPLETE_GENOMICS	ss167452180	Jul 04, 2010 (132)
22	ILLUMINA	ss171612527	Jul 04, 2010 (132)
23	ILLUMINA	ss173614150	Jul 04, 2010 (132)
24	BUSHMAN	ss202693959	Jul 04, 2010 (132)
25	1000GENOMES	ss222799705	Jul 14, 2010 (132)
26	1000GENOMES	ss233771460	Jul 15, 2010 (132)
27	1000GENOMES	ss240767879	Jul 15, 2010 (132)
28	GMI	ss285542040	Apr 25, 2013 (138)
29	PJP	ss293777033	May 09, 2011 (134)
30	ILLUMINA	ss410929656	Sep 17, 2011 (135)
31	ILLUMINA	ss480803408	May 04, 2012 (137)
32	ILLUMINA	ss480819159	May 04, 2012 (137)
33	ILLUMINA	ss481745372	Sep 08, 2015 (146)
34	ILLUMINA	ss485196491	May 04, 2012 (137)
35	ILLUMINA	ss536133922	Sep 08, 2015 (146)
36	SSMP	ss654017278	Apr 25, 2013 (138)
37	ILLUMINA	ss778893399	Sep 08, 2015 (146)
38	ILLUMINA	ss783044288	Aug 21, 2014 (142)
39	ILLUMINA	ss784003357	Sep 08, 2015 (146)
40	ILLUMINA	ss825493896	Apr 01, 2015 (144)
41	ILLUMINA	ss832302057	Apr 01, 2015 (144)
42	ILLUMINA	ss832951913	Aug 21, 2014 (142)
43	ILLUMINA	ss833542742	Aug 21, 2014 (142)
44	ILLUMINA	ss834354550	Sep 08, 2015 (146)
45	EVA-GONL	ss983738200	Aug 21, 2014 (142)
46	JMKIDD_LAB	ss1074213762	Aug 21, 2014 (142)
47	1000GENOMES	ss1323177451	Aug 21, 2014 (142)
48	EVA_GENOME_DK	ss1581987626	Apr 01, 2015 (144)
49	EVA_DECODE	ss1593314597	Apr 01, 2015 (144)
50	EVA_UK10K_ALSPAC	ss1617185680	Apr 01, 2015 (144)
51	EVA_UK10K_TWINSUK	ss1660179713	Apr 01, 2015 (144)
52	EVA_SVP	ss1712917560	Apr 01, 2015 (144)
53	ILLUMINA	ss1752613585	Sep 08, 2015 (146)
54	WEILL_CORNELL_DGM	ss1926980124	Feb 12, 2016 (147)
55	JJLAB	ss2024156663	Sep 14, 2016 (149)
56	USC_VALOUEV	ss2152350106	Dec 20, 2016 (150)
57	HUMAN_LONGEVITY	ss2290261327	Dec 20, 2016 (150)
58	ILLUMINA	ss2634540768	Nov 08, 2017 (151)
59	GNOMAD	ss2847672098	Nov 08, 2017 (151)
60	AFFY	ss2986021645	Nov 08, 2017 (151)
61	SWEGEN	ss3000311933	Nov 08, 2017 (151)
62	BIOINF_KMB_FNS_UNIBA	ss3025869518	Nov 08, 2017 (151)
63	CSHL	ss3347333068	Nov 08, 2017 (151)
64	ILLUMINA	ss3629708213	Oct 12, 2018 (152)
65	ILLUMINA	ss3632452303	Oct 12, 2018 (152)
66	ILLUMINA	ss3633445814	Oct 12, 2018 (152)
67	ILLUMINA	ss3634169776	Oct 12, 2018 (152)
68	ILLUMINA	ss3635099388	Oct 12, 2018 (152)
69	ILLUMINA	ss3635850028	Oct 12, 2018 (152)
70	ILLUMINA	ss3636828406	Oct 12, 2018 (152)
71	ILLUMINA	ss3637602934	Oct 12, 2018 (152)
72	ILLUMINA	ss3638670205	Oct 12, 2018 (152)
73	ILLUMINA	ss3639336644	Oct 12, 2018 (152)
74	ILLUMINA	ss3639695699	Oct 12, 2018 (152)
75	ILLUMINA	ss3640806689	Oct 12, 2018 (152)
76	ILLUMINA	ss3643608351	Oct 12, 2018 (152)
77	OMUKHERJEE_ADBS	ss3646346550	Oct 12, 2018 (152)
78	EGCUT_WGS	ss3668250593	Jul 13, 2019 (153)
79	EVA_DECODE	ss3718722871	Jul 13, 2019 (153)
80	ACPOP	ss3734182637	Jul 13, 2019 (153)
81	ILLUMINA	ss3745399300	Jul 13, 2019 (153)
82	EVA	ss3765949068	Jul 13, 2019 (153)
83	ILLUMINA	ss3772892600	Jul 13, 2019 (153)
84	KHV_HUMAN_GENOMES	ss3809112809	Jul 13, 2019 (153)
85	EVA	ss3825711202	Apr 26, 2020 (154)
86	EVA	ss3830308867	Apr 26, 2020 (154)
87	HGDP	ss3847859247	Apr 26, 2020 (154)
88	SGDP_PRJ	ss3866188247	Apr 26, 2020 (154)
89	KRGDB	ss3913180527	Apr 26, 2020 (154)
90	KOGIC	ss3960510325	Apr 26, 2020 (154)
91	FSA-LAB	ss3984354310	Apr 26, 2021 (155)
92	EVA	ss3985266716	Apr 26, 2021 (155)
93	EVA	ss4017311531	Apr 26, 2021 (155)
94	TOPMED	ss4729539749	Apr 26, 2021 (155)
95	TOMMO_GENOMICS	ss5180942206	Apr 26, 2021 (155)
96	1000G_HIGH_COVERAGE	ss5271145073	Oct 13, 2022 (156)
97	EVA	ss5315207905	Oct 13, 2022 (156)
98	EVA	ss5370456328	Oct 13, 2022 (156)
99	HUGCELL_USP	ss5468517174	Oct 13, 2022 (156)
100	1000G_HIGH_COVERAGE	ss5558479213	Oct 13, 2022 (156)
101	SANFORD_IMAGENETICS	ss5641948127	Oct 13, 2022 (156)
102	TOMMO_GENOMICS	ss5720117746	Oct 13, 2022 (156)
103	EVA	ss5799709535	Oct 13, 2022 (156)
104	YY_MCH	ss5808154689	Oct 13, 2022 (156)
105	EVA	ss5843301286	Oct 13, 2022 (156)
106	EVA	ss5886871610	Oct 13, 2022 (156)
107	EVA	ss5971020098	Oct 13, 2022 (156)
108	EVA	ss5971020099	Oct 13, 2022 (156)
109	1000Genomes	NC_000006.11 - 161769835	Oct 12, 2018 (152)
110	1000Genomes_30x	NC_000006.12 - 161348803	Oct 13, 2022 (156)
111	The Avon Longitudinal Study of Parents and Children	NC_000006.11 - 161769835	Oct 12, 2018 (152)
112	Chileans	NC_000006.11 - 161769835	Apr 26, 2020 (154)
113	Genetic variation in the Estonian population	NC_000006.11 - 161769835	Oct 12, 2018 (152)
114	The Danish reference pan genome	NC_000006.11 - 161769835	Apr 26, 2020 (154)
115	gnomAD - Genomes	NC_000006.12 - 161348803	Apr 26, 2021 (155)
116	Genome of the Netherlands Release 5	NC_000006.11 - 161769835	Apr 26, 2020 (154)
117	HGDP-CEPH-db Supplement 1	NC_000006.10 - 161689825	Apr 26, 2020 (154)
118	HapMap	NC_000006.12 - 161348803	Apr 26, 2020 (154)
119	KOREAN population from KRGDB	NC_000006.11 - 161769835	Apr 26, 2020 (154)
120	Korean Genome Project	NC_000006.12 - 161348803	Apr 26, 2020 (154)
121	Northern Sweden	NC_000006.11 - 161769835	Jul 13, 2019 (153)
122	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000006.11 - 161769835	Apr 26, 2021 (155)
123	Qatari	NC_000006.11 - 161769835	Apr 26, 2020 (154)
124	SGDP_PRJ	NC_000006.11 - 161769835	Apr 26, 2020 (154)
125	Siberian	NC_000006.11 - 161769835	Apr 26, 2020 (154)
126	8.3KJPN	NC_000006.11 - 161769835	Apr 26, 2021 (155)
127	14KJPN	NC_000006.12 - 161348803	Oct 13, 2022 (156)
128	TopMed	NC_000006.12 - 161348803	Apr 26, 2021 (155)
129	UK 10K study - Twins	NC_000006.11 - 161769835	Oct 12, 2018 (152)
130	ALFA	NC_000006.12 - 161348803	Apr 26, 2021 (155)
131	ClinVar	RCV000376877.3	Oct 13, 2022 (156)

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)
rs17629437	Oct 08, 2004 (123)
rs60673545	May 26, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss3639336644, ss3639695699	NC_000006.9:161740245:T:C	NC_000006.12:161348802:T:C	(self)
537139, ss66430441, ss76202864, ss93595443, ss160632621, ss167452180, ss202693959, ss285542040, ss293777033, ss410929656, ss480803408, ss825493896, ss1593314597, ss1712917560, ss3643608351, ss3847859247	NC_000006.10:161689824:T:C	NC_000006.12:161348802:T:C	(self)
35080885, 19565657, 396812, 13988841, 8152565, 8707260, 20357921, 7467502, 492643, 9022054, 18205227, 4866460, 38911513, 19565657, ss222799705, ss233771460, ss240767879, ss480819159, ss481745372, ss485196491, ss536133922, ss654017278, ss778893399, ss783044288, ss784003357, ss832302057, ss832951913, ss833542742, ss834354550, ss983738200, ss1074213762, ss1323177451, ss1581987626, ss1617185680, ss1660179713, ss1752613585, ss1926980124, ss2024156663, ss2152350106, ss2634540768, ss2847672098, ss2986021645, ss3000311933, ss3347333068, ss3629708213, ss3632452303, ss3633445814, ss3634169776, ss3635099388, ss3635850028, ss3636828406, ss3637602934, ss3638670205, ss3640806689, ss3646346550, ss3668250593, ss3734182637, ss3745399300, ss3765949068, ss3772892600, ss3825711202, ss3830308867, ss3866188247, ss3913180527, ss3984354310, ss3985266716, ss4017311531, ss5180942206, ss5315207905, ss5370456328, ss5641948127, ss5799709535, ss5843301286, ss5971020098, ss5971020099	NC_000006.11:161769834:T:C	NC_000006.12:161348802:T:C	(self)
RCV000376877.3, 46005148, 247622134, 3299231, 16888326, 53954850, 566917307, 4138407321, ss2290261327, ss3025869518, ss3718722871, ss3809112809, ss3960510325, ss4729539749, ss5271145073, ss5468517174, ss5558479213, ss5720117746, ss5808154689, ss5886871610	NC_000006.12:161348802:T:C	NC_000006.12:161348802:T:C	(self)
ss4920461, ss24470215, ss66746334, ss67297745, ss67702284, ss68998891, ss70776373, ss71352451, ss75696494, ss79163378, ss84159737, ss99307790, ss122200086, ss142474102, ss154263471, ss159440336, ss171612527, ss173614150	NT_025741.15:65939291:T:C	NC_000006.12:161348802:T:C	(self)

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

1 citation for rs3734464

PMID	Title	Author	Year	Journal
24419040	Response to Belgard et al.	Skafidas E et al.	2014	Molecular psychiatry

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

rs3734464