Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4822489
rs4822489
Entrez Id: 135;646023;101730217
Gene Symbol: ADORA2A;ADORA2A-AS1;SPECC1L-ADORA2A
ADORA2A;ADORA2A-AS1;SPECC1L-ADORA2A
CUI: C0018802
Disease:
Congestive heart failure
0.010 GeneticVariation BEFREE The findings of this study suggest that rs4822489 may contribute to the severity of CHF in the northern Chinese. 25629231 2015