rs2009262

Parent Gene: PNPT1

Importance: 5
Less common allele: C = 30%
More common allele: T = 70%
My Genotype: Log In
Risk Allele: T

Disease/Trait: Inguinal Hernia

The T allele of rs2009262 is reported to be associated with Inguinal Hernia . Your genotype was not identified for this SNP so we are unable to comment on your association with Inguinal hernia.