Source: BEFREE

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs868443937
rs868443937
ING1
CUI: C0025202
Disease: melanoma
melanoma 		0.010 GeneticVariation BEFREE We show that 20% of the melanoma primaries contained missense mutations in the SAP30-interacting domain and PHD finger motif of the ING1 gene with the R102L and N260S alterations observed more than once. 15201991

2004