Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11016879
rs11016879
0.010 GeneticVariation BEFREE The MGMT rs11016879 AG genotype and A allele were associated with increased HNSCC risk. 29370316

2018

dbSNP: rs12917
rs12917
0.010 GeneticVariation BEFREE Our results indicated that the MGMT rs12917 TT genotype increases the risk of HNSCC. 29370316

2018