Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1805009
rs1805009
Entrez Id: 4157;10381
Gene Symbol: MC1R;TUBB3
MC1R;TUBB3
CUI: C0268495
Disease:
Oculocutaneous albinism type 2
C 0.700 GeneticVariation CLINVAR Identification and functional characterization of natural human melanocortin 1 receptor mutant alleles in Pakistani population. 26197705 2015