MYH7B, myosin heavy chain 7B, 57644

N. diseases: 18; N. variants: 20
Disease: melanoma ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0025202
Disease: melanoma
melanoma 		0.110 GeneticVariation disease GWASCAT Two-stage genome-wide association study identifies a novel susceptibility locus associated with melanoma. 28212542 2017
CUI: C0025202
Disease: melanoma
melanoma 		0.110 GeneticVariation disease BEFREE Eight loci were identified in the main meta-analyses as being associated with a risk of CM (P < .05) of which four loci showed a genome-wide statistically significant association (P < 1 × 10(-7)), including 16q24.3 (MC1R), 20q11.22 (MYH7B/PIGU/ASIP), 11q14.3 (TYR), and 5p13.2 (SLC45A2). 21693730 2011
CUI: C0025202
Disease: melanoma
melanoma 		0.110 GeneticVariation disease GWASDB Common sequence variants on 20q11.22 confer melanoma susceptibility. 18488026 2008