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rs4686760

From SNPedia

Orientationplus
Stabilizedplus
Make rs4686760(A;A)
Make rs4686760(A;G)
Make rs4686760(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position184796825
is asnp
is mentioned by
dbSNPrs4686760
ClinGenrs4686760
ebirs4686760
HLIrs4686760
Exacrs4686760
Varsomers4686760
Maprs4686760
PheGenIrs4686760
hapmaprs4686760
1000 genomesrs4686760
hgdprs4686760
ensemblrs4686760
gopubmedrs4686760
geneviewrs4686760
scholarrs4686760
googlers4686760
pharmgkbrs4686760
gwascentralrs4686760
openSNPrs4686760
23andMers4686760
23andMe allrs4686760
SNP Nexus

SNPshotrs4686760
SNPdbers4686760
MSV3drs4686760
GWAS Ctlgrs4686760
GMAF0.3627
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 21810271OA-icon.png]
Trait
Title Combined analysis of three genome-wide association studies on vWF and FVIII plasma levels.
Risk Allele G
P-val 0.000001
Odds Ratio 0.1500 [0.09-0.21] IU/dL decrease