NEXN, nexilin F-actin binding protein, 91624

N. diseases: 36; N. variants: 8
Disease: CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 20 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs387907079
rs387907079
Entrez Id: 91624
Gene Symbol: NEXN
NEXN
CUI: C3151267
Disease:
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 20 		0.800 GeneticVariation UNIPROT Mutations in NEXN, a Z-disc gene, are associated with hypertrophic cardiomyopathy. 20970104 2010
dbSNP: rs387907079
rs387907079
Entrez Id: 91624
Gene Symbol: NEXN
NEXN
CUI: C3151267
Disease:
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 20 		G 0.800 CausalMutation CLINVAR