rs138163892, PITX2

N. diseases: 2
Disease: Atrial Fibrillation ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Atrial Fibrillation
CUI: C0004238
Disease: Atrial Fibrillation
0.010 GeneticVariation BEFREE These conditions may contribute to the propensity to AF found in patients carrying the p.Met207Val variant. 30558760 2019