rs55670112

Parent Gene: TRIM36

Importance: 3
Less common allele: C = 47%
More common allele: A = 53%
My Genotype: Log In
Risk Allele: C

Disease/Trait: Generalised Epilepsy

The C allele of rs55670112 is reported to be associated with Generalised Epilepsy (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Epilepsy (GGE).