Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121965074
rs121965074
FAH
CUI: C0268483
Disease: Tyrosinemias
Tyrosinemias 		0.010 GeneticVariation BEFREE An Ala 134 to Asp (GCT to GAT) transition was found in one Turkish and two Norwegian patients with chronic tyrosinemia. 8005583

1994