Name: rs1367634
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.

rs1367634

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr18:53338298 (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>G
Variation Type: SNV Single Nucleotide Variation
Frequency: T=0.391243 (103558/264690, TOPMED)
T=0.371741 (89878/241776, ALFA)
T=0.368579 (51607/140016, GnomAD) (+ 18 more)
T=0.44358 (34897/78672, PAGE_STUDY)
G=0.35105 (9920/28258, 14KJPN)
G=0.35137 (5889/16760, 8.3KJPN)
T=0.4600 (2946/6404, 1000G_30x)
T=0.4665 (2336/5008, 1000G)
T=0.2734 (1225/4480, Estonian)
T=0.4001 (1542/3854, ALSPAC)
T=0.3867 (1434/3708, TWINSUK)
G=0.3860 (1131/2930, KOREAN)
T=0.4174 (788/1888, HapMap)
T=0.398 (397/998, GoNL)
G=0.449 (342/762, PRJEB37584)
T=0.330 (198/600, NorthernSweden)
T=0.308 (127/412, SGDP_PRJ)
T=0.384 (83/216, Qatari)
T=0.481 (102/212, Vietnamese)
T=0.25 (11/44, Siberian)
T=0.42 (17/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: DCC : Intron Variant
Publications: 2 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	246810	T=0.371735	G=0.628265
European	Sub	223864	T=0.365155	G=0.634845
African	Sub	8382	T=0.3194	G=0.6806
African Others	Sub	350	T=0.314	G=0.686
African American	Sub	8032	T=0.3196	G=0.6804
Asian	Sub	3832	T=0.5929	G=0.4071
East Asian	Sub	3106	T=0.6033	G=0.3967
Other Asian	Sub	726	T=0.548	G=0.452
Latin American 1	Sub	966	T=0.362	G=0.638
Latin American 2	Sub	2548	T=0.5950	G=0.4050
South Asian	Sub	350	T=0.537	G=0.463
Other	Sub	6868	T=0.4368	G=0.5632

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=0.391243	G=0.608757
Allele Frequency Aggregator	Total	Global	241776	T=0.371741	G=0.628259
Allele Frequency Aggregator	European	Sub	220770	T=0.365059	G=0.634941
Allele Frequency Aggregator	African	Sub	7240	T=0.3182	G=0.6818
Allele Frequency Aggregator	Other	Sub	6070	T=0.4372	G=0.5628
Allele Frequency Aggregator	Asian	Sub	3832	T=0.5929	G=0.4071
Allele Frequency Aggregator	Latin American 2	Sub	2548	T=0.5950	G=0.4050
Allele Frequency Aggregator	Latin American 1	Sub	966	T=0.362	G=0.638
Allele Frequency Aggregator	South Asian	Sub	350	T=0.537	G=0.463
gnomAD - Genomes	Global	Study-wide	140016	T=0.368579	G=0.631421
gnomAD - Genomes	European	Sub	75838	T=0.35594	G=0.64406
gnomAD - Genomes	African	Sub	41956	T=0.32115	G=0.67885
gnomAD - Genomes	American	Sub	13630	T=0.50902	G=0.49098
gnomAD - Genomes	Ashkenazi Jewish	Sub	3320	T=0.4636	G=0.5364
gnomAD - Genomes	East Asian	Sub	3126	T=0.5784	G=0.4216
gnomAD - Genomes	Other	Sub	2146	T=0.3979	G=0.6021
The PAGE Study	Global	Study-wide	78672	T=0.44358	G=0.55642
The PAGE Study	AfricanAmerican	Sub	32508	T=0.32158	G=0.67842
The PAGE Study	Mexican	Sub	10804	T=0.63078	G=0.36922
The PAGE Study	Asian	Sub	8316	T=0.6257	G=0.3743
The PAGE Study	PuertoRican	Sub	7916	T=0.4266	G=0.5734
The PAGE Study	NativeHawaiian	Sub	4534	T=0.5337	G=0.4663
The PAGE Study	Cuban	Sub	4228	T=0.3813	G=0.6187
The PAGE Study	Dominican	Sub	3824	T=0.3583	G=0.6417
The PAGE Study	CentralAmerican	Sub	2450	T=0.5747	G=0.4253
The PAGE Study	SouthAmerican	Sub	1978	T=0.6112	G=0.3888
The PAGE Study	NativeAmerican	Sub	1258	T=0.4475	G=0.5525
The PAGE Study	SouthAsian	Sub	856	T=0.544	G=0.456
14KJPN	JAPANESE	Study-wide	28258	T=0.64895	G=0.35105
8.3KJPN	JAPANESE	Study-wide	16760	T=0.64863	G=0.35137
1000Genomes_30x	Global	Study-wide	6404	T=0.4600	G=0.5400
1000Genomes_30x	African	Sub	1786	T=0.3068	G=0.6932
1000Genomes_30x	Europe	Sub	1266	T=0.3705	G=0.6295
1000Genomes_30x	South Asian	Sub	1202	T=0.5815	G=0.4185
1000Genomes_30x	East Asian	Sub	1170	T=0.5675	G=0.4325
1000Genomes_30x	American	Sub	980	T=0.578	G=0.422
1000Genomes	Global	Study-wide	5008	T=0.4665	G=0.5335
1000Genomes	African	Sub	1322	T=0.3048	G=0.6952
1000Genomes	East Asian	Sub	1008	T=0.5694	G=0.4306
1000Genomes	Europe	Sub	1006	T=0.3748	G=0.6252
1000Genomes	South Asian	Sub	978	T=0.593	G=0.407
1000Genomes	American	Sub	694	T=0.579	G=0.421
Genetic variation in the Estonian population	Estonian	Study-wide	4480	T=0.2734	G=0.7266
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	T=0.4001	G=0.5999
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	T=0.3867	G=0.6133
KOREAN population from KRGDB	KOREAN	Study-wide	2930	T=0.6140	G=0.3860
HapMap	Global	Study-wide	1888	T=0.4174	G=0.5826
HapMap	American	Sub	770	T=0.484	G=0.516
HapMap	African	Sub	690	T=0.257	G=0.743
HapMap	Asian	Sub	252	T=0.675	G=0.325
HapMap	Europe	Sub	176	T=0.386	G=0.614
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	T=0.398	G=0.602
CNV burdens in cranial meningiomas	Global	Study-wide	762	T=0.551	G=0.449
CNV burdens in cranial meningiomas	CRM	Sub	762	T=0.551	G=0.449
Northern Sweden	ACPOP	Study-wide	600	T=0.330	G=0.670
SGDP_PRJ	Global	Study-wide	412	T=0.308	G=0.692
Qatari	Global	Study-wide	216	T=0.384	G=0.616
A Vietnamese Genetic Variation Database	Global	Study-wide	212	T=0.481	G=0.519
Siberian	Global	Study-wide	44	T=0.25	G=0.75
The Danish reference pan genome	Danish	Study-wide	40	T=0.42	G=0.57

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 18	NC_000018.10:g.53338298T>G
GRCh37.p13 chr 18	NC_000018.9:g.50864668T>G
DCC RefSeqGene (LRG_1107)	NG_013341.2:g.1003127T>G

Gene: DCC, DCC netrin 1 receptor (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
DCC transcript	NM_005215.4:c.2165-1415T>G	N/A	Intron Variant
DCC transcript variant X4	XM_011525844.3:c.1130-141… XM_011525844.3:c.1130-1415T>G	N/A	Intron Variant
DCC transcript variant X1	XM_017025568.2:c.2165-141… XM_017025568.2:c.2165-1415T>G	N/A	Intron Variant
DCC transcript variant X2	XM_017025569.2:c.2165-141… XM_017025569.2:c.2165-1415T>G	N/A	Intron Variant
DCC transcript variant X3	XM_047437311.1:c.2165-141… XM_047437311.1:c.2165-1415T>G	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	T=	G
GRCh38.p14 chr 18	NC_000018.10:g.53338298=	NC_000018.10:g.53338298T>G
GRCh37.p13 chr 18	NC_000018.9:g.50864668=	NC_000018.9:g.50864668T>G
DCC RefSeqGene (LRG_1107)	NG_013341.2:g.1003127=	NG_013341.2:g.1003127T>G
DCC transcript	NM_005215.3:c.2165-1415=	NM_005215.3:c.2165-1415T>G
DCC transcript	NM_005215.4:c.2165-1415=	NM_005215.4:c.2165-1415T>G
DCC transcript variant X1	XM_005258204.1:c.2165-1415=	XM_005258204.1:c.2165-1415T>G
DCC transcript variant X4	XM_011525844.3:c.1130-1415=	XM_011525844.3:c.1130-1415T>G
DCC transcript variant X1	XM_017025568.2:c.2165-1415=	XM_017025568.2:c.2165-1415T>G
DCC transcript variant X2	XM_017025569.2:c.2165-1415=	XM_017025569.2:c.2165-1415T>G
DCC transcript variant X3	XM_047437311.1:c.2165-1415=	XM_047437311.1:c.2165-1415T>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#.

120 SubSNP, 21 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	TSC-CSHL	ss2153185	Oct 23, 2000 (88)
2	BCM_SSAHASNP	ss10910944	Jul 11, 2003 (116)
3	SSAHASNP	ss21493525	Apr 05, 2004 (121)
4	PERLEGEN	ss24089853	Sep 20, 2004 (123)
5	ABI	ss44122241	Mar 14, 2006 (126)
6	ILLUMINA	ss65775210	Oct 16, 2006 (127)
7	ILLUMINA	ss75018016	Dec 06, 2007 (129)
8	HGSV	ss79863056	Dec 14, 2007 (130)
9	BCMHGSC_JDW	ss90797981	Mar 24, 2008 (129)
10	HUMANGENOME_JCVI	ss96342569	Feb 04, 2009 (130)
11	1000GENOMES	ss110565041	Jan 25, 2009 (130)
12	1000GENOMES	ss114423143	Jan 25, 2009 (130)
13	ILLUMINA-UK	ss117882908	Feb 14, 2009 (130)
14	KRIBB_YJKIM	ss119389628	Dec 01, 2009 (131)
15	ENSEMBL	ss136403725	Dec 01, 2009 (131)
16	ENSEMBL	ss137390588	Dec 01, 2009 (131)
17	GMI	ss155200704	Dec 01, 2009 (131)
18	ILLUMINA	ss160342686	Dec 01, 2009 (131)
19	COMPLETE_GENOMICS	ss168265343	Jul 04, 2010 (132)
20	COMPLETE_GENOMICS	ss169862667	Jul 04, 2010 (132)
21	ILLUMINA	ss172447230	Jul 04, 2010 (132)
22	BUSHMAN	ss203297719	Jul 04, 2010 (132)
23	BCM-HGSC-SUB	ss208085504	Jul 04, 2010 (132)
24	1000GENOMES	ss227881302	Jul 14, 2010 (132)
25	1000GENOMES	ss237481765	Jul 15, 2010 (132)
26	1000GENOMES	ss243728422	Jul 15, 2010 (132)
27	BL	ss255677270	May 09, 2011 (134)
28	GMI	ss283005392	May 04, 2012 (137)
29	PJP	ss292076252	May 09, 2011 (134)
30	ILLUMINA	ss479942969	May 04, 2012 (137)
31	ILLUMINA	ss479951265	May 04, 2012 (137)
32	ILLUMINA	ss480588898	Sep 08, 2015 (146)
33	ILLUMINA	ss484769730	May 04, 2012 (137)
34	ILLUMINA	ss536859523	Sep 08, 2015 (146)
35	TISHKOFF	ss565665310	Apr 25, 2013 (138)
36	SSMP	ss661499448	Apr 25, 2013 (138)
37	ILLUMINA	ss778428820	Aug 21, 2014 (142)
38	ILLUMINA	ss782831575	Sep 08, 2015 (146)
39	ILLUMINA	ss783796373	Aug 21, 2014 (142)
40	ILLUMINA	ss832085080	Sep 08, 2015 (146)
41	ILLUMINA	ss833884272	Aug 21, 2014 (142)
42	EVA-GONL	ss993770007	Aug 21, 2014 (142)
43	JMKIDD_LAB	ss1081531143	Aug 21, 2014 (142)
44	1000GENOMES	ss1361190053	Aug 21, 2014 (142)
45	DDI	ss1428229692	Apr 01, 2015 (144)
46	EVA_GENOME_DK	ss1578420819	Apr 01, 2015 (144)
47	EVA_UK10K_ALSPAC	ss1636964718	Apr 01, 2015 (144)
48	EVA_UK10K_TWINSUK	ss1679958751	Apr 01, 2015 (144)
49	EVA_DECODE	ss1697831055	Apr 01, 2015 (144)
50	EVA_SVP	ss1713629220	Apr 01, 2015 (144)
51	ILLUMINA	ss1752259697	Sep 08, 2015 (146)
52	HAMMER_LAB	ss1809068623	Sep 08, 2015 (146)
53	WEILL_CORNELL_DGM	ss1937237647	Feb 12, 2016 (147)
54	ILLUMINA	ss1946504272	Feb 12, 2016 (147)
55	ILLUMINA	ss1959807388	Feb 12, 2016 (147)
56	GENOMED	ss1968533310	Jul 19, 2016 (147)
57	JJLAB	ss2029388621	Sep 14, 2016 (149)
58	USC_VALOUEV	ss2157895517	Dec 20, 2016 (150)
59	HUMAN_LONGEVITY	ss2221914370	Dec 20, 2016 (150)
60	SYSTEMSBIOZJU	ss2629192152	Nov 08, 2017 (151)
61	ILLUMINA	ss2633478088	Nov 08, 2017 (151)
62	GRF	ss2702485564	Nov 08, 2017 (151)
63	ILLUMINA	ss2710869401	Nov 08, 2017 (151)
64	GNOMAD	ss2957148727	Nov 08, 2017 (151)
65	SWEGEN	ss3016592528	Nov 08, 2017 (151)
66	ILLUMINA	ss3021846953	Nov 08, 2017 (151)
67	BIOINF_KMB_FNS_UNIBA	ss3028523336	Nov 08, 2017 (151)
68	CSHL	ss3352041656	Nov 08, 2017 (151)
69	ILLUMINA	ss3625726234	Oct 12, 2018 (152)
70	ILLUMINA	ss3627818540	Oct 12, 2018 (152)
71	ILLUMINA	ss3631454487	Oct 12, 2018 (152)
72	ILLUMINA	ss3633164062	Oct 12, 2018 (152)
73	ILLUMINA	ss3633872907	Oct 12, 2018 (152)
74	ILLUMINA	ss3634707883	Oct 12, 2018 (152)
75	ILLUMINA	ss3635560156	Oct 12, 2018 (152)
76	ILLUMINA	ss3636397279	Oct 12, 2018 (152)
77	ILLUMINA	ss3637311773	Oct 12, 2018 (152)
78	ILLUMINA	ss3638198449	Oct 12, 2018 (152)
79	ILLUMINA	ss3640415191	Oct 12, 2018 (152)
80	ILLUMINA	ss3641090262	Oct 12, 2018 (152)
81	ILLUMINA	ss3641385829	Oct 12, 2018 (152)
82	ILLUMINA	ss3643173998	Oct 12, 2018 (152)
83	ILLUMINA	ss3644706770	Oct 12, 2018 (152)
84	URBANLAB	ss3650799266	Oct 12, 2018 (152)
85	ILLUMINA	ss3652269039	Oct 12, 2018 (152)
86	EGCUT_WGS	ss3683436856	Jul 13, 2019 (153)
87	EVA_DECODE	ss3701740055	Jul 13, 2019 (153)
88	ILLUMINA	ss3725680067	Jul 13, 2019 (153)
89	ACPOP	ss3742578335	Jul 13, 2019 (153)
90	ILLUMINA	ss3744159335	Jul 13, 2019 (153)
91	ILLUMINA	ss3745008026	Jul 13, 2019 (153)
92	EVA	ss3755441554	Jul 13, 2019 (153)
93	PAGE_CC	ss3771974301	Jul 13, 2019 (153)
94	ILLUMINA	ss3772505499	Jul 13, 2019 (153)
95	PACBIO	ss3788381549	Jul 13, 2019 (153)
96	PACBIO	ss3793311332	Jul 13, 2019 (153)
97	PACBIO	ss3798197716	Jul 13, 2019 (153)
98	KHV_HUMAN_GENOMES	ss3820698656	Jul 13, 2019 (153)
99	EVA	ss3835189549	Apr 27, 2020 (154)
100	EVA	ss3841212256	Apr 27, 2020 (154)
101	EVA	ss3846714539	Apr 27, 2020 (154)
102	SGDP_PRJ	ss3887103387	Apr 27, 2020 (154)
103	KRGDB	ss3936984551	Apr 27, 2020 (154)
104	EVA	ss3984733472	Apr 26, 2021 (155)
105	EVA	ss4017800338	Apr 26, 2021 (155)
106	TOPMED	ss5058150775	Apr 26, 2021 (155)
107	TOMMO_GENOMICS	ss5225355271	Apr 26, 2021 (155)
108	1000G_HIGH_COVERAGE	ss5305434696	Oct 16, 2022 (156)
109	EVA	ss5315936373	Oct 16, 2022 (156)
110	HUGCELL_USP	ss5498190408	Oct 16, 2022 (156)
111	EVA	ss5511953482	Oct 16, 2022 (156)
112	1000G_HIGH_COVERAGE	ss5610352872	Oct 16, 2022 (156)
113	SANFORD_IMAGENETICS	ss5661375526	Oct 16, 2022 (156)
114	TOMMO_GENOMICS	ss5783199037	Oct 16, 2022 (156)
115	EVA	ss5799994736	Oct 16, 2022 (156)
116	YY_MCH	ss5817133505	Oct 16, 2022 (156)
117	EVA	ss5827600478	Oct 16, 2022 (156)
118	EVA	ss5852070293	Oct 16, 2022 (156)
119	EVA	ss5874249331	Oct 16, 2022 (156)
120	EVA	ss5952796599	Oct 16, 2022 (156)
121	1000Genomes	NC_000018.9 - 50864668	Oct 12, 2018 (152)
122	1000Genomes_30x	NC_000018.10 - 53338298	Oct 16, 2022 (156)
123	The Avon Longitudinal Study of Parents and Children	NC_000018.9 - 50864668	Oct 12, 2018 (152)
124	Genetic variation in the Estonian population	NC_000018.9 - 50864668	Oct 12, 2018 (152)
125	The Danish reference pan genome	NC_000018.9 - 50864668	Apr 27, 2020 (154)
126	gnomAD - Genomes	NC_000018.10 - 53338298	Apr 26, 2021 (155)
127	Genome of the Netherlands Release 5	NC_000018.9 - 50864668	Apr 27, 2020 (154)
128	HapMap	NC_000018.10 - 53338298	Apr 27, 2020 (154)
129	KOREAN population from KRGDB	NC_000018.9 - 50864668	Apr 27, 2020 (154)
130	Northern Sweden	NC_000018.9 - 50864668	Jul 13, 2019 (153)
131	The PAGE Study	NC_000018.10 - 53338298	Jul 13, 2019 (153)
132	CNV burdens in cranial meningiomas	NC_000018.9 - 50864668	Apr 26, 2021 (155)
133	Qatari	NC_000018.9 - 50864668	Apr 27, 2020 (154)
134	SGDP_PRJ	NC_000018.9 - 50864668	Apr 27, 2020 (154)
135	Siberian	NC_000018.9 - 50864668	Apr 27, 2020 (154)
136	8.3KJPN	NC_000018.9 - 50864668	Apr 26, 2021 (155)
137	14KJPN	NC_000018.10 - 53338298	Oct 16, 2022 (156)
138	TopMed	NC_000018.10 - 53338298	Apr 26, 2021 (155)
139	UK 10K study - Twins	NC_000018.9 - 50864668	Oct 12, 2018 (152)
140	A Vietnamese Genetic Variation Database	NC_000018.9 - 50864668	Jul 13, 2019 (153)
141	ALFA	NC_000018.10 - 53338298	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)
rs57189003	May 23, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss79863056, ss90797981, ss110565041, ss114423143, ss117882908, ss160342686, ss168265343, ss169862667, ss203297719, ss208085504, ss255677270, ss283005392, ss292076252, ss479942969, ss1697831055, ss1713629220, ss3643173998	NC_000018.8:49118665:T:G	NC_000018.10:53338297:T:G	(self)
74524699, 41296456, 29175104, 4612132, 18396811, 44161945, 15863200, 283024, 19279569, 39120367, 10411871, 83324578, 41296456, 9124418, ss227881302, ss237481765, ss243728422, ss479951265, ss480588898, ss484769730, ss536859523, ss565665310, ss661499448, ss778428820, ss782831575, ss783796373, ss832085080, ss833884272, ss993770007, ss1081531143, ss1361190053, ss1428229692, ss1578420819, ss1636964718, ss1679958751, ss1752259697, ss1809068623, ss1937237647, ss1946504272, ss1959807388, ss1968533310, ss2029388621, ss2157895517, ss2629192152, ss2633478088, ss2702485564, ss2710869401, ss2957148727, ss3016592528, ss3021846953, ss3352041656, ss3625726234, ss3627818540, ss3631454487, ss3633164062, ss3633872907, ss3634707883, ss3635560156, ss3636397279, ss3637311773, ss3638198449, ss3640415191, ss3641090262, ss3641385829, ss3644706770, ss3652269039, ss3683436856, ss3742578335, ss3744159335, ss3745008026, ss3755441554, ss3772505499, ss3788381549, ss3793311332, ss3798197716, ss3835189549, ss3841212256, ss3887103387, ss3936984551, ss3984733472, ss4017800338, ss5225355271, ss5315936373, ss5511953482, ss5661375526, ss5799994736, ss5827600478, ss5952796599	NC_000018.9:50864667:T:G	NC_000018.10:53338297:T:G	(self)
97878807, 525720551, 1610554, 1195770, 117036141, 273696438, 971279032, ss2221914370, ss3028523336, ss3650799266, ss3701740055, ss3725680067, ss3771974301, ss3820698656, ss3846714539, ss5058150775, ss5305434696, ss5498190408, ss5610352872, ss5783199037, ss5817133505, ss5852070293, ss5874249331	NC_000018.10:53338297:T:G	NC_000018.10:53338297:T:G	(self)
ss10910944, ss21493525	NT_010966.13:32353769:T:G	NC_000018.10:53338297:T:G	(self)
ss2153185, ss24089853, ss44122241, ss65775210, ss75018016, ss96342569, ss119389628, ss136403725, ss137390588, ss155200704, ss172447230	NT_010966.14:32353769:T:G	NC_000018.10:53338297:T:G	(self)

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

2 citations for rs1367634

PMID	Title	Author	Year	Journal
21197116	Genome-wide association analyses of genetic, phenotypic, and environmental risks in the age-related eye disease study.	Ryu E et al.	2010	Molecular vision
25132797	Using current data to define new approach in age related macular degeneration: need to accelerate translational research.	Anand A et al.	2014	Current genomics

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

rs1367634