rs318497

Orientation

plus

Stabilized

plus

Make rs318497(A;A)

Make rs318497(A;G)

Make rs318497(G;G)

Reference

GRCh38 38.1/141

Chromosome

6

Position

2912043

is a	snp
is	mentioned by
dbSNP	rs318497
dbSNP (classic)	rs318497
ClinGen	rs318497
ebi	rs318497
HLI	rs318497
Exac	rs318497
Gnomad	rs318497
Varsome	rs318497
LitVar	rs318497
Map	rs318497
PheGenI	rs318497
Biobank	rs318497
1000 genomes	rs318497
hgdp	rs318497
ensembl	rs318497
geneview	rs318497
scholar	rs318497
google	rs318497
pharmgkb	rs318497
gwascentral	rs318497
openSNP	rs318497
23andMe	rs318497
SNPshot	rs318497
SNPdbe	rs318497
MSV3d	rs318497
GWAS Ctlg	rs318497

GMAF

0.4793

Max Magnitude

0

?	(A;A) (A;G) (G;G)	28

GWAS snp
PMID	[PMID 23509962]
Trait	Venous thromboembolism (gene x gene interaction)
Title	A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosis.
Risk Allele
P-val	5E-9
Odds Ratio	2.33 [NR]