rs1800693

Parent Gene: TNFRSF1A

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

Disease/Trait: Multiple Sclerosis

The C allele of rs1800693 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: Biliary Liver Cirrhosis

The C allele of rs1800693 is reported to be associated with Biliary Liver Cirrhosis (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Primary biliary cholangitis.

Disease/Trait: Multiple Sclerosis

The G allele of rs1800693 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 C allele of rs1800693 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.