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.
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.827 0.200 6 32373576 intron variant G/A snv 0.45 0.800 1.000 1 2012 2012
Sarcoidosis
CUI: C0036202
Disease: Sarcoidosis
787 0.827 0.200 6 32373576 intron variant G/A snv 0.45 0.700 1.000 2 2008 2012
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.827 0.200 6 32373576 intron variant G/A snv 0.45 0.700 1.000 1 2007 2007
Narcolepsy
CUI: C0027404
Disease: Narcolepsy
454 0.827 0.200 6 32373576 intron variant G/A snv 0.45 0.700 1.000 1 2009 2009
Cardiomyopathy, Familial Idiopathic
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
243 0.827 0.200 6 32373576 intron variant G/A snv 0.45 0.010 1.000 1 2015 2015