rs4239633, UNC13A

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.
Benign Prostatic Hyperplasia
CUI: C1704272
Disease: Benign Prostatic Hyperplasia
91 0.851 0.240 19 17631660 intron variant C/T snv 0.32 0.700 1.000 1 2019 2019
Amyotrophic Lateral Sclerosis
CUI: C0002736
Disease: Amyotrophic Lateral Sclerosis
485 0.851 0.240 19 17631660 intron variant C/T snv 0.32 0.010 1.000 1 2018 2018
Frontotemporal dementia
CUI: C0338451
Disease: Frontotemporal dementia
215 0.851 0.240 19 17631660 intron variant C/T snv 0.32 0.010 1.000 1 2018 2018
Progressive supranuclear palsy
CUI: C0038868
Disease: Progressive supranuclear palsy
52 0.851 0.240 19 17631660 intron variant C/T snv 0.32 0.010 1.000 1 2018 2018