rs10166942

Parent Gene: MSL3P1, TRPM8

Importance: 3
Less common allele: T = 46%
More common allele: C = 54%
My Genotype: Log In
Risk Allele: T

Disease/Trait: Migraine Disorder

The T allele of rs10166942 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.

Disease/Trait: Migraine Disorder

rs10166942 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

rs10166942 is associated with Migraine Disorder (R) . It is reported to increased association with Migraine. No specific risk allele was identified in the study.