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 Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.882 0.040 5 151022235 intron variant A/G snv 0.67 0.010 1.000 1 2019 2019
Differentiated Thyroid Gland Carcinoma
CUI: C1337013
Disease: Differentiated Thyroid Gland Carcinoma
80 0.882 0.040 5 151022235 intron variant A/G snv 0.67 0.010 1.000 1 2009 2009
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.882 0.040 5 151022235 intron variant A/G snv 0.67 0.010 1.000 1 2011 2011
Hypertriglyceridemia
CUI: C0020557
Disease: Hypertriglyceridemia
169 0.882 0.040 5 151022235 intron variant A/G snv 0.67 0.010 1.000 1 2019 2019
Primary differentiated carcinoma of thyroid gland
CUI: C4722172
Disease: Primary differentiated carcinoma of thyroid gland
41 0.882 0.040 5 151022235 intron variant A/G snv 0.67 0.010 1.000 1 2009 2009