rs2932538, MOV10

N. diseases: 4
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
0.810 GeneticVariation BEFREE SNP rs2932538, a variant in MOV10, was found to be significantly associated with an increased risk of hypertension. 24338417 2013
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
0.810 GeneticVariation GWASDB Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk. 21909115 2011
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
0.810 GeneticVariation GWASCAT Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk. 21909115 2011