Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
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: rs6052751
rs6052751
Entrez Id: 92507
Gene Symbol: RPS4XP2
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: rs1029273
rs1029273
Entrez Id: 92507
Gene Symbol: RPS4XP2
RPS4XP2
CUI: C1852467
Disease:
Creutzfeldt-Jakob Disease, Sporadic
0.010 GeneticVariation BEFREE In addition, at a single nucleotide polymorphism upstream of PRNP thought to confer susceptibility to sporadic Creutzfeldt-Jakob disease (rs1029273), all patients were homozygous for the risk allele (combined P=5.9×10(-5)). 21616973 2011
dbSNP: rs6052761
rs6052761
Entrez Id: 92507
Gene Symbol: RPS4XP2
RPS4XP2
CUI: C0004096
Disease:
Asthma
0.010 GeneticVariation BEFREE A meta-analysis combining these 2 African-ancestry populations yielded 3 SNPs with a combined P value of less than 10(-5) in genes of potential biologic relevance to asthma and allergic disease: rs10515807, mapping to the alpha-1B-adrenergic receptor (ADRA1B) gene on chromosome 5q33 (3.57 x 10(-6)); rs6052761, mapping to the prion-related protein (PRNP) gene on chromosome 20pter-p12 (2.27 x 10(-6)); and rs1435879, mapping to the dipeptidyl peptidase 10 (DPP10) gene on chromosome 2q12.3-q14.2. 19910028 2010