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: rs146245480
rs146245480
NEXN
CUI: C3151267
Disease: CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 20
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 20 		T 0.800 CausalMutation CLINVAR

dbSNP: rs387907079
rs387907079
NEXN
CUI: C3151267
Disease: CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 20
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 20 		G 0.800 CausalMutation CLINVAR

dbSNP: rs137853197
rs137853197
NEXN
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated 		G 0.700 GeneticVariation CLINVAR Nexilin mutations destabilize cardiac Z-disks and lead to dilated cardiomyopathy. 19881492

2009
dbSNP: rs137853197
rs137853197
NEXN
CUI: C1834481
Disease: CARDIOMYOPATHY, DILATED, 1S
CARDIOMYOPATHY, DILATED, 1S 		G 0.700 GeneticVariation CLINVAR

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