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rs4979078

From SNPedia

Orientationplus
Stabilizedplus
Make rs4979078(C;C)
Make rs4979078(C;T)
Make rs4979078(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position112060841
GeneSUSD1
is asnp
is mentioned by
dbSNPrs4979078
ebirs4979078
HLIrs4979078
Exacrs4979078
Varsomers4979078
Maprs4979078
PheGenIrs4979078
hapmaprs4979078
1000 genomesrs4979078
hgdprs4979078
ensemblrs4979078
gopubmedrs4979078
geneviewrs4979078
scholarrs4979078
googlers4979078
pharmgkbrs4979078
gwascentralrs4979078
openSNPrs4979078
23andMers4979078
23andMe allrs4979078
SNP Nexus

SNPshotrs4979078
SNPdbers4979078
MSV3drs4979078
GWAS Ctlgrs4979078
GMAF0.2893
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23650146OA-icon.png]
Trait Venous thromboembolism
Title A genome-wide association study for venous thromboembolism: the extended cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium.
Risk Allele C
P-val 3E-6
Odds Ratio 1.21 [1.11-1.30]