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.
Sudden infant death syndrome
CUI: C0038644
Disease: Sudden infant death syndrome
68 0.851 0.200 18 26866562 intron variant G/A snv 0.31 0.020 1.000 2 2010 2014
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.851 0.200 18 26866562 intron variant G/A snv 0.31 0.010 1.000 1 2015 2015
Meniere Disease
CUI: C0025281
Disease: Meniere Disease
36 0.851 0.200 18 26866562 intron variant G/A snv 0.31 0.010 1.000 1 2013 2013
Neuromyelitis Optica
CUI: C0027873
Disease: Neuromyelitis Optica
45 0.851 0.200 18 26866562 intron variant G/A snv 0.31 0.010 1.000 1 2016 2016
Sudden sensorineural hearing loss
CUI: C4275242
Disease: Sudden sensorineural hearing loss
38 0.851 0.200 18 26866562 intron variant G/A snv 0.31 0.010 1.000 1 2013 2013