Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Migraine Disorders
CUI: C0149931
Disease: Migraine Disorders
0.010 GeneticVariation BEFREE This suggests that mutant alleles of C314T for HNMT and C2029G for DAO polymorphisms may interact in a way that increases the risk and impact of migraine. 27130307 2017