rs7937106

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(T;T)	0	common genotype

Make rs7937106(C;C)

Make rs7937106(C;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

107483586

is a	snp
is	mentioned by
dbSNP	rs7937106
dbSNP (classic)	rs7937106
ClinGen	rs7937106
ebi	rs7937106
HLI	rs7937106
Exac	rs7937106
Gnomad	rs7937106
Varsome	rs7937106
LitVar	rs7937106
Map	rs7937106
PheGenI	rs7937106
Biobank	rs7937106
1000 genomes	rs7937106
hgdp	rs7937106
ensembl	rs7937106
geneview	rs7937106
scholar	rs7937106
google	rs7937106
pharmgkb	rs7937106
gwascentral	rs7937106
openSNP	rs7937106
23andMe	rs7937106
SNPshot	rs7937106
SNPdbe	rs7937106
MSV3d	rs7937106
GWAS Ctlg	rs7937106

Max Magnitude

0

?	(C;C) (C;T) (T;T)	28

GWAS snp
PMID	[PMID 24262325]
Trait	Large artery stroke
Title	Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants.
Risk Allele	C
P-val	6E-8
Odds Ratio	1.69 [1.40-2.04]