rs1816, KANSL1

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.
Familial (FPAH)
CUI: C1611743
Disease: Familial (FPAH)
276 0.882 0.200 17 46199252 intron variant A/G snv 0.14 0.010 1.000 1 2002 2002
Frontotemporal dementia
CUI: C0338451
Disease: Frontotemporal dementia
215 0.882 0.200 17 46199252 intron variant A/G snv 0.14 0.010 1.000 1 2002 2002
Progressive supranuclear palsy
CUI: C0038868
Disease: Progressive supranuclear palsy
52 0.882 0.200 17 46199252 intron variant A/G snv 0.14 0.010 1.000 1 2002 2002