Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4822489
rs4822489
ADORA2A ; ADORA2A-AS1 ; SPECC1L-ADORA2A
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