rs17608902

Parent Gene: FBN2

Importance: 3
Less common allele: A = 5%
More common allele: C = 95%
My Genotype: Log In
Risk Allele: A, A

Disease/Trait: Migraine Disorder

The A allele of rs17608902 is reported to be associated with Migraine Disorder (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Migraine with aura.

Disease/Trait: Migraine Disorder

The A allele of rs17608902 is reported to be associated with Migraine Disorder (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Migraine - clinic-based.