Gene: MIR155 ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs767649
rs767649
MIR155HG ; MIR155
0.010 GeneticVariation BEFREE In conclusion, rs767649 might be a causal variant for CC susceptibility. 27717891

2016