rs6604026  was significantly associated with multiple sclerosis (MS) (P=0.041) [RR1].

 

 

rs6604026

Parent Gene: FAM69A, RPL5

Importance: 4
Less common allele: C = 19%
More common allele: T = 81%
My Genotype: Log In
Risk Allele: C, G

Disease/Trait: Multiple Sclerosis

The C allele of rs6604026 is reported to be associated with Multiple Sclerosis (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Multiple sclerosis.

Disease/Trait: Multiple Sclerosis

The G allele of rs6604026 is reported to be associated with Multiple Sclerosis (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Multiple sclerosis.