rs6687758, None

N. diseases: 11
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
0.810 GeneticVariation BEFREE Our findings validate the known association of loci at MAPT, MOBP, EIF2AK3 and STX6 with risk of PSP, and uncover novel associations with SLCO1A2 (rs11568563) and DUSP10 (rs6687758) variants, both of which were classified as non-significant in the original GWAS. 29986742 2018
Progressive supranuclear palsy
CUI: C0038868
Disease: Progressive supranuclear palsy
0.810 GeneticVariation GWASCAT Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy. 21685912 2011
Progressive supranuclear palsy
CUI: C0038868
Disease: Progressive supranuclear palsy
0.810 GeneticVariation GWASDB Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy. 21685912 2011