rs2471738, STH;MAPT

N. diseases: 4
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.
Intelligence
CUI: C0021704
Disease: Intelligence
2093 0.882 0.160 17 45998697 intron variant C/T snv 0.18 0.700 1.000 2 2018 2018
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.882 0.160 17 45998697 intron variant C/T snv 0.18 0.030 1.000 3 2009 2017
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.882 0.160 17 45998697 intron variant C/T snv 0.18 0.010 1.000 1 2017 2017
Progressive supranuclear palsy
CUI: C0038868
Disease: Progressive supranuclear palsy
52 0.882 0.160 17 45998697 intron variant C/T snv 0.18 0.010 1.000 1 2017 2017