rs393152

Parent Gene: CRHR1, CRHR1-IT1, MGC57346-CRHR1

Importance: 3
Less common allele: G = 25%
More common allele: A = 75%
My Genotype: Log In
Risk Allele: A

Disease/Trait: Parkinson's Disease

The A allele of rs393152 is reported to be associated with Parkinson's Disease (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Parkinson's disease.

Disease/Trait: Corticobasal Degeneration

rs393152 is associated with Corticobasal Degeneration (R) . It is reported to increased association with Corticobasal degeneration. No specific risk allele was identified in the study.