Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs796051880
rs796051880
TYR ; LOC107984363
T 0.700 GeneticVariation CLINVAR Sequence analysis of tyrosinase gene in ocular and oculocutaneous albinism patients: introducing three novel mutations. 26167114

2015
dbSNP: rs104894314
rs104894314
TYR ; LOC107984363
0.010 GeneticVariation BEFREE One patient is homozygous for the previously known V275F mutation but has an extremely mild OCA phenotype and has no eye features typical of OCA. 11295837

2001