[PMID 19081515] Genetic risk factors for variant Creutzfeldt-Jakob disease: a genome-wide association study.

rs6107516

Parent Gene: PRNP

Importance: 3
Less common allele: A = 18%
More common allele: G = 82%
My Genotype: Log In
Risk Allele: C

Disease/Trait: Creutzfeldt Jacob Disease

rs6107516 is associated with Creutzfeldt Jacob Disease (R) . It is reported to association with Creutzfeldt-Jakob disease (variant). No specific risk allele was identified in the study.

Disease/Trait: Sporadic Creutzfeld Jacob Disease

The C allele of rs6107516 is reported to be associated with Sporadic Creutzfeld Jacob Disease (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Creutzfeldt-Jakob disease (sporadic).