rs6695352

Parent Gene: CENPF

Importance: 3
Less common allele: T = 37%
More common allele: C = 63%
My Genotype: Log In
Risk Allele:

Disease/Trait: Migraine Disorder

rs6695352 is associated with Migraine Disorder (R) . It is reported to increased association with Migraine without aura. No specific risk allele was identified in the study.