The C (major) allele is associated with:

  • CC= Increased risk of multiple sclerosis (MS)
  • CC= Increased risk of Type 1 Diabetes.

rs6897932

Parent Gene: IL7R, TREGS

Importance: 5
Less common allele: T = 17%
More common allele: C = 83%
My Genotype: Log In
Risk Allele: C, G, C, G, T

Disease/Trait: Multiple Sclerosis

The C allele of rs6897932 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: Type I Diabetes Mellitus

The G allele of rs6897932 is reported to be associated with Type I Diabetes Mellitus (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Type 1 diabetes.

Disease/Trait: Multiple Sclerosis

The C allele of rs6897932 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 rs6897932 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: Primary Biliary Cirrhosis

The T allele of rs6897932 is reported to be associated with Primary Biliary Cirrhosis (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Primary biliary cholangitis.