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rs4253399

From SNPedia

Orientationplus
Stabilizedplus
Make rs4253399(G;G)
Make rs4253399(G;T)
Make rs4253399(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position186266940
GeneF11
is asnp
is mentioned by
dbSNPrs4253399
ebirs4253399
HLIrs4253399
Exacrs4253399
Varsomers4253399
Maprs4253399
PheGenIrs4253399
hapmaprs4253399
1000 genomesrs4253399
hgdprs4253399
ensemblrs4253399
gopubmedrs4253399
geneviewrs4253399
scholarrs4253399
googlers4253399
pharmgkbrs4253399
gwascentralrs4253399
openSNPrs4253399
23andMers4253399
23andMe allrs4253399
SNP Nexus

SNPshotrs4253399
SNPdbers4253399
MSV3drs4253399
GWAS Ctlgrs4253399
GMAF0.2833
Max Magnitude
? (G;G) (G;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 G
P-val 3E-14
Odds Ratio 1.24 [1.17-1.31]