rs6430538

Parent Gene: ACMSD, TMEM163

Importance: 3
Less common allele: C = 19%
More common allele: T = 81%
My Genotype: Log In
Risk Allele: C

Disease/Trait: Parkinson's Disease

rs6430538 is associated with Parkinson's Disease (R) . It is reported to increased association with Parkinson's disease. No specific risk allele was identified in the study.

Disease/Trait: Parkinson's Disease

The C allele of rs6430538 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.