rs1411478, STX6

N. diseases: 3
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 0.925 0.120 1 180993146 intron variant A/G snv 0.56 0.810 1.000 2 2011 2013
Age at menopause
CUI: C1629609
Disease: Age at menopause
209 0.925 0.120 1 180993146 intron variant A/G snv 0.56 0.700 1.000 1 2015 2015
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.925 0.120 1 180993146 intron variant A/G snv 0.56 0.010 1 2013 2013