rs11613092

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in complete genomics

Make rs11613092(C;T)

Make rs11613092(T;T)

Reference

GRCh38 38.1/141

Chromosome

12

Position

118455443

is a	snp
is	mentioned by
dbSNP	rs11613092
dbSNP (classic)	rs11613092
ClinGen	rs11613092
ebi	rs11613092
HLI	rs11613092
Exac	rs11613092
Gnomad	rs11613092
Varsome	rs11613092
LitVar	rs11613092
Map	rs11613092
PheGenI	rs11613092
Biobank	rs11613092
1000 genomes	rs11613092
hgdp	rs11613092
ensembl	rs11613092
geneview	rs11613092
scholar	rs11613092
google	rs11613092
pharmgkb	rs11613092
gwascentral	rs11613092
openSNP	rs11613092
23andMe	rs11613092
SNPshot	rs11613092
SNPdbe	rs11613092
MSV3d	rs11613092
GWAS Ctlg	rs11613092

GMAF

0.1088

Max Magnitude

0

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

GWAS snp
PMID	[PMID 22443383]
Trait
Title	Genome wide association study for plasma levels of natural anticoagulant inhibitors and protein C anticoagulant pathway: the MARTHA project.
Risk Allele	T
P-val	0.000006
Odds Ratio	8.1600 None