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rs6858430

From SNPedia

Orientationplus
Stabilizedplus
Make rs6858430(C;C)
Make rs6858430(C;T)
Make rs6858430(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position174894978
is asnp
is mentioned by
dbSNPrs6858430
dbSNP (classic)rs6858430
ClinGenrs6858430
ebirs6858430
HLIrs6858430
Exacrs6858430
Gnomadrs6858430
Varsomers6858430
LitVarrs6858430
Maprs6858430
PheGenIrs6858430
Biobankrs6858430
1000 genomesrs6858430
hgdprs6858430
ensemblrs6858430
geneviewrs6858430
scholarrs6858430
googlers6858430
pharmgkbrs6858430
gwascentralrs6858430
openSNPrs6858430
23andMers6858430
SNPshotrs6858430
SNPdbers6858430
MSV3drs6858430
GWAS Ctlgrs6858430
GMAF0.3338
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 23509962OA-icon.png]
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 G
P-val 1E-8
Odds Ratio 1.62 [NR]