PRNP, prion protein, 5621

N. diseases: 2; N. variants: 3
Source: GWASDB ×
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1799990
rs1799990
Entrez Id: 5621
Gene Symbol: PRNP
PRNP
CUI: C0022336
Disease:
Creutzfeldt-Jakob disease 		A 0.900 GeneticVariation GWASDB Genetic risk factors for variant Creutzfeldt-Jakob disease: a genome-wide association study. 19081515 2009
dbSNP: rs1799990
rs1799990
Entrez Id: 5621
Gene Symbol: PRNP
PRNP
CUI: C0162534
Disease:
Prion Diseases 		0.860 GeneticVariation GWASDB Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP. 22210626 2012
dbSNP: rs6107516
rs6107516
Entrez Id: 5621
Gene Symbol: PRNP
PRNP
CUI: C0022336
Disease:
Creutzfeldt-Jakob disease 		0.800 GeneticVariation GWASDB Genome-wide study links MTMR7 gene to variant Creutzfeldt-Jakob risk. 22137330 2012
dbSNP: rs2756271
rs2756271
Entrez Id: 5621;92507
Gene Symbol: PRNP;RPS4XP2
PRNP;RPS4XP2
CUI: C0162534
Disease:
Prion Diseases 		0.700 GeneticVariation GWASDB Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP. 22210626 2012
dbSNP: rs6107516
rs6107516
Entrez Id: 5621
Gene Symbol: PRNP
PRNP
CUI: C0162534
Disease:
Prion Diseases 		0.700 GeneticVariation GWASDB Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP. 22210626 2012