Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121918086
rs121918086
TTR
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies 		0.010 GeneticVariation BEFREE Cardiomyopathy in a Japanese family with the Glu61Lys transthyretin variant: a new phenotype. 20536403

2009