Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104894313
rs104894313
TYR ; LOC107984363
0.800 GeneticVariation UNIPROT Novel and recurrent mutations in the tyrosinase gene and the P gene in the German albino population. 10987646

1999
dbSNP: rs104894313
rs104894313
TYR ; LOC107984363
0.800 GeneticVariation UNIPROT Mutations of the tyrosinase gene in patients with oculocutaneous albinism from various ethnic groups in Israel. 8128955

1994
dbSNP: rs104894313
rs104894313
TYR ; LOC107984363
0.800 GeneticVariation UNIPROT "Tyrosinase gene mutations associated with type IB (""yellow"") oculocutaneous albinism." 1903591

1991
dbSNP: rs104894313
rs104894313
TYR ; LOC107984363
0.800 GeneticVariation UNIPROT A tyrosinase gene missense mutation in temperature-sensitive type I oculocutaneous albinism. A human homologue to the Siamese cat and the Himalayan mouse. 1900309

1991
dbSNP: rs104894313
rs104894313
TYR ; LOC107984363
T 0.800 CausalMutation CLINVAR

dbSNP: rs104894313
rs104894313
TYR ; LOC107984363
T 0.800 GeneticVariation CLINVAR