Disease: Familial neurocardiogenic syncope ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Familial neurocardiogenic syncope
CUI: C1836438
Disease: Familial neurocardiogenic syncope
0.010 GeneticVariation BEFREE Adenosine A(2A) receptor 1083 T > C polymorphism is not associated with the positivity of HUT and its proposed role in predisposition to VVS was not confirmed. 26710963 2016