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.