Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10249788
rs10249788
AHR ; LOC101927609
0.010 GeneticVariation BEFREE However, no significant differences were observed in allele and genotype frequencies of rs2066853 and rs10249788 between patients with CD and the controls (all <i>p</i> > 0.05). 31405308

2019