Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs137853197
rs137853197
NEXN
CUI: C2751084
Disease: Cardiomyopathy, Dilated, 1CC
Cardiomyopathy, Dilated, 1CC 		G 0.800 CausalMutation CLINVAR

dbSNP: rs137853198
rs137853198
NEXN
CUI: C2751084
Disease: Cardiomyopathy, Dilated, 1CC
Cardiomyopathy, Dilated, 1CC 		A 0.800 CausalMutation CLINVAR

dbSNP: rs771262904
rs771262904
NEXN
CUI: C2751084
Disease: Cardiomyopathy, Dilated, 1CC
Cardiomyopathy, Dilated, 1CC 		T 0.700 GeneticVariation CLINVAR