Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs775488556
rs775488556
Tyrosine Transaminase Deficiency Disease
T 0.700 GeneticVariation CLINVAR Novel and recurrent tyrosine aminotransferase gene mutations in tyrosinemia type II. 9544843

1998