Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs398122917
rs398122917
C 0.800 CausalMutation CLINVAR

dbSNP: rs398122917
rs398122917
0.800 GeneticVariation UNIPROT An X-linked channelopathy with cardiomegaly due to a CLIC2 mutation enhancing ryanodine receptor channel activity. 22814392

2012