rs10849061

Parent Gene: FGF23, FGF6

Importance: 3
Less common allele: T = 34%
More common allele: C = 66%
My Genotype: Log In
Risk Allele:

Disease/Trait: Migraine Disorder

rs10849061 is associated with Migraine Disorder (R) . It is reported to increased association with Migraine. No specific risk allele was identified in the study.

Disease/Trait: Migraine Disorder

rs10849061 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.

Disease/Trait: Migraine Disorder

rs10849061 is associated with Migraine Disorder (R) . It is reported to increased association with Migraine - clinic-based. No specific risk allele was identified in the study.