Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3824120
rs3824120
Entrez Id: 4609;100270680
Gene Symbol: MYC;CASC11
MYC;CASC11
CUI: C0006826
Disease:
Malignant Neoplasms
0.010 GeneticVariation BEFREE We determined that one SNP allele (rs3824120) in a CpG island associated with MYC which eliminated a CpG was more common in the cancer datasets than in the 100Genomes databases (p < 0.01). 27074591 2016