PRND, prion like protein doppel, 23627

N. diseases: 27; N. variants: 3
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2245220
rs2245220
Entrez Id: 23627
Gene Symbol: PRND
PRND
CUI: C1852467
Disease:
Creutzfeldt-Jakob Disease, Sporadic 		0.010 GeneticVariation BEFREE No significant association of PRND T174M with sCJD was shown. 17047093 2006
dbSNP: rs2245220
rs2245220
Entrez Id: 23627
Gene Symbol: PRND
PRND
CUI: C0022336
Disease:
Creutzfeldt-Jakob disease 		0.010 GeneticVariation BEFREE The meta-analysis on the PRND T174M polymorphism did not show a consistent effect across studies, raising the question as to whether PRND 174M is causally related to CJD, or whether the PRND allele is in linkage disequilibrium with another polymorphism related to CJD. 14970845 2004
dbSNP: rs2245220
rs2245220
Entrez Id: 23627
Gene Symbol: PRND
PRND
CUI: C4310512
Disease:
Sporadic CJD 		0.010 GeneticVariation BEFREE We further found a significant increased prevalence of M homozygotes at PRND T174M among sporadic CJD patients, when adjusting the analyses for the other genotypes. 14970845 2004
dbSNP: rs35453518
rs35453518
Entrez Id: 23627
Gene Symbol: PRND
PRND
CUI: C0022336
Disease:
Creutzfeldt-Jakob disease 		0.010 GeneticVariation BEFREE We investigated the role of a single-nucleotide polymorphism (SNP 1368) located upstream of PRNP and three polymorphisms in PRND (T26M, P56L and T174M) in CJD. 14970845 2004
dbSNP: rs41279424
rs41279424
Entrez Id: 23627
Gene Symbol: PRND
PRND
CUI: C0022336
Disease:
Creutzfeldt-Jakob disease 		0.010 GeneticVariation BEFREE We investigated the role of a single-nucleotide polymorphism (SNP 1368) located upstream of PRNP and three polymorphisms in PRND (T26M, P56L and T174M) in CJD. 14970845 2004