rs1768208, MOBP

N. diseases: 4
Disease: Progressive supranuclear palsy ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Progressive supranuclear palsy
CUI: C0038868
Disease: Progressive supranuclear palsy
0.830 GeneticVariation BEFREE Meta-analysis revealed highly significant associations for PSP risk alleles of rs8070723 and rs1768208 with higher LRRC37A4 and MOBP brain levels, respectively. 27115769 2016
Progressive supranuclear palsy
CUI: C0038868
Disease: Progressive supranuclear palsy
0.830 GeneticVariation BEFREE Testing for association of CBD with top progressive supranuclear palsy (PSP) GWAS single-nucleotide polymorphisms (SNPs) identified associations at MOBP (3p22; rs1768208; P=2.07 × 10(-7)) and MAPT H1c (17q21; rs242557; P=7.91 × 10(-6)). 26077951 2015
Progressive supranuclear palsy
CUI: C0038868
Disease: Progressive supranuclear palsy
0.830 GeneticVariation BEFREE An SNP (rs1768208 C/T) has been identified as a strong risk factor for PSP. 26335643 2015
Progressive supranuclear palsy
CUI: C0038868
Disease: Progressive supranuclear palsy
0.830 GeneticVariation GWASDB Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy. 21685912 2011
Progressive supranuclear palsy
CUI: C0038868
Disease: Progressive supranuclear palsy
0.830 GeneticVariation GWASCAT Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy. 21685912 2011