rs1861960

Parent Gene: CNPY1, EN2

Importance: 3
Less common allele: T = 35%
More common allele: G = 65%
My Genotype: Log In
Risk Allele: T

Disease/Trait: Migraine Disorder

The T allele of rs1861960 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.