Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121918097
rs121918097
TTR
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies 		0.010 GeneticVariation BEFREE Cardiomyopathy in Swedish patients with the Gly53Glu and His88Arg transthyretin variants. 16194874

2005