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rs1757948

From SNPedia

Orientationminus
Stabilizedminus
Make rs1757948(G;G)
Make rs1757948(G;T)
Make rs1757948(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position78695764
is asnp
is mentioned by
dbSNPrs1757948
ebirs1757948
HLIrs1757948
Exacrs1757948
Varsomers1757948
Maprs1757948
PheGenIrs1757948
hapmaprs1757948
1000 genomesrs1757948
hgdprs1757948
ensemblrs1757948
gopubmedrs1757948
geneviewrs1757948
scholarrs1757948
googlers1757948
pharmgkbrs1757948
gwascentralrs1757948
openSNPrs1757948
23andMers1757948
23andMe allrs1757948
SNP Nexus

SNPshotrs1757948
SNPdbers1757948
MSV3drs1757948
GWAS Ctlgrs1757948
GMAF0.2902
Max Magnitude
? (G;G) (G;T) (T;T) 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 0.000007
Odds Ratio 0.1500 [0.09-0.21] IU/dL increase