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.
Glaucoma
CUI: C0017601
Disease: Glaucoma
209 0.846 0.107 9 22032153 intron variant T/G snp 0.30 0.700 1 2012 2012
Malignant Central Nervous System Neoplasm
87 0.846 0.107 9 22032153 intron variant T/G snp 0.30 0.700 1 2017 2017
Glioblastoma Multiforme
CUI: C1621958
Disease: Glioblastoma Multiforme
42 0.846 0.107 9 22032153 intron variant T/G snp 0.30 0.700 1 2017 2017
Glioma
CUI: C0017638
Disease: Glioma
180 0.846 0.107 9 22032153 intron variant T/G snp 0.30 0.700 1 2017 2017
Calcification of coronary artery
CUI: C1611184
Disease: Calcification of coronary artery
3393 0.846 0.107 9 22032153 intron variant T/G snp 0.30 0.700 1 2012 2012