rs17375901 was associated with increased scar risk in atrial fibrillation (AF) patients (OR 3.68, p=0.03) [R].
 

rs17375901

Parent Gene: MTHFR

Importance: 3
Less common allele: T = 3%
More common allele: C = 97%
My Genotype: Log In
Risk Allele: T

Disease/Trait: Atrial Fibrillation

The T allele of rs17375901 is reported to be associated with Atrial Fibrillation (R). Your genotype was not identified for this SNP so we are unable to comment on your association with Atrial fibrillation.