rs12446487

Parent Gene: CNOT1, SLC38A7

Importance: 3
Less common allele: C = 28%
More common allele: A = 72%
My Genotype: Log In
Risk Allele: C

Disease/Trait: Schizophrenia

The C allele of rs12446487 is reported to be associated with Schizophrenia (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Schizophrenia.