Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1883832
rs1883832
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders
0.010 GeneticVariation BEFREE Our findings showed that in CD40 rs1883832, TC genotype may have a role in migraine susceptibility. 30511624

2018