Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs267599211
rs267599211
Entrez Id: 9125
Gene Symbol: CNOT9
CNOT9
CUI: C0025202
Disease:
melanoma
0.010 GeneticVariation BEFREE Whole exome sequencing identifies a recurrent RQCD1 P131L mutation in cutaneous melanoma. 25544760 2015