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rs11613092

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs11613092(C;T)
Make rs11613092(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position118455443
is asnp
is mentioned by
dbSNPrs11613092
ebirs11613092
HLIrs11613092
Exacrs11613092
Varsomers11613092
Maprs11613092
PheGenIrs11613092
hapmaprs11613092
1000 genomesrs11613092
hgdprs11613092
ensemblrs11613092
gopubmedrs11613092
geneviewrs11613092
scholarrs11613092
googlers11613092
pharmgkbrs11613092
gwascentralrs11613092
openSNPrs11613092
23andMers11613092
23andMe allrs11613092
SNP Nexus

SNPshotrs11613092
SNPdbers11613092
MSV3drs11613092
GWAS Ctlgrs11613092
GMAF0.1088
Max Magnitude0
? (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