rs1805007, MC1R

N. diseases: 25
Disease: Melanosis ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Melanosis
CUI: C0025209
Disease: Melanosis
0.700 GeneticVariation GWASCAT Multitrait genome association analysis identifies new susceptibility genes for human anthropometric variation in the GCAT cohort. 30166351 2018
Melanosis
CUI: C0025209
Disease: Melanosis
0.700 GeneticVariation GWASCAT Genetic determinants of hair, eye and skin pigmentation in Europeans. 17952075 2007