rs10675541, MOBP

N. diseases: 1
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Progressive supranuclear palsy
CUI: C0038868
Disease: Progressive supranuclear palsy
52 1.000 0.120 3 39468795 intron variant -/CA delins 0.700 1.000 1 2018 2018