Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs9547996
rs9547996
Entrez Id: 7223
Gene Symbol: TRPC4
TRPC4
CUI: C0428883
Disease:
Diastolic blood pressure
G 0.700 GeneticVariation GWASCAT Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk. 28135244 2017
dbSNP: rs9547991
rs9547991
Entrez Id: 7223
Gene Symbol: TRPC4
TRPC4
CUI: C0014859
Disease:
Esophageal Neoplasms
0.700 GeneticVariation GWASDB Genome-wide association analyses of esophageal squamous cell carcinoma in Chinese identify multiple susceptibility loci and gene-environment interactions. 22960999 2012
dbSNP: rs73184536
rs73184536
Entrez Id: 7223
Gene Symbol: TRPC4
TRPC4
CUI: C0027051
Disease:
Myocardial Infarction
0.010 GeneticVariation BEFREE Our candidate-gene association studies identified a missense SNP (TRPC4-I957V) associated with a reduced risk of MI in diabetic patients [odds ratio (OR) = 0.61; confidence interval (CI), 0.40-0.95, P= 0.02]. 21427121 2011
dbSNP: rs7319926
rs7319926
Entrez Id: 7223
Gene Symbol: TRPC4
TRPC4
CUI: C0027051
Disease:
Myocardial Infarction
0.010 GeneticVariation BEFREE TRPC4 was also associated with MI in the Wellcome Trust Case-Control Consortium's genome-wide data: an intronic SNP (rs7319926) within the same linkage disequilibrium block as TRPC4-I957V showed an OR of 0.86 (CI, 0.81-0.94; P =10(-4)). 21427121 2011