Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs72648250
rs72648250
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2J
A 0.700 CausalMutation CLINVAR Titin Truncating Variants in Dilated Cardiomyopathy - Prevalence and Genotype-Phenotype Correlations. 28045975

2017

dbSNP: rs72648250
rs72648250
CUI: C1858763
Disease: Cardiomyopathy, Dilated, 1g
Cardiomyopathy, Dilated, 1g
A 0.700 CausalMutation CLINVAR Titin Truncating Variants in Dilated Cardiomyopathy - Prevalence and Genotype-Phenotype Correlations. 28045975

2017

dbSNP: rs72648250
rs72648250
CUI: C1858763
Disease: Cardiomyopathy, Dilated, 1g
Cardiomyopathy, Dilated, 1g
A 0.700 CausalMutation CLINVAR Integrated allelic, transcriptional, and phenomic dissection of the cardiac effects of titin truncations in health and disease. 25589632

2015

dbSNP: rs72648250
rs72648250
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2J
A 0.700 CausalMutation CLINVAR Integrated allelic, transcriptional, and phenomic dissection of the cardiac effects of titin truncations in health and disease. 25589632

2015

dbSNP: rs72648250
rs72648250
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2J
A 0.700 CausalMutation CLINVAR Recessive truncating titin gene, TTN, mutations presenting as centronuclear myopathy. 23975875

2013

dbSNP: rs72648250
rs72648250
CUI: C1858763
Disease: Cardiomyopathy, Dilated, 1g
Cardiomyopathy, Dilated, 1g
A 0.700 CausalMutation CLINVAR Recessive truncating titin gene, TTN, mutations presenting as centronuclear myopathy. 23975875

2013

dbSNP: rs72648250
rs72648250
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2J
A 0.700 CausalMutation CLINVAR Truncations of titin causing dilated cardiomyopathy. 22335739

2012

dbSNP: rs72648250
rs72648250
CUI: C1858763
Disease: Cardiomyopathy, Dilated, 1g
Cardiomyopathy, Dilated, 1g
A 0.700 CausalMutation CLINVAR Truncations of titin causing dilated cardiomyopathy. 22335739

2012

dbSNP: rs72648250
rs72648250
CUI: C0340427
Disease: Familial dilated cardiomyopathy
Familial dilated cardiomyopathy
A 0.700 CausalMutation CLINVAR

dbSNP: rs72648250
rs72648250
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated
A 0.700 GeneticVariation CLINVAR