rs121913506, KIT

N. diseases: 24
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Seminoma
CUI: C0036631
Disease: Seminoma
0.010 GeneticVariation BEFREE A novel missense mutation (D816H) was found in the phosphotransferase domain in tumors of seminoma/dysgerminoma differentiation. 10362788 1999