Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs13175330
rs13175330
Entrez Id: 5066
Gene Symbol: PAM
PAM
CUI: C0020538
Disease:
Hypertensive disease
0.010 GeneticVariation BEFREE These results suggest that the PAM rs13175330 A>G SNP is a novel candidate gene for HTN in the Korean population. 29162152 2017