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.
Malignant Central Nervous System Neoplasm
87 0.801 0.321 9 22043927 intron variant A/G snp 0.30 0.800 3 2009 2011
Nasopharyngeal Neoplasms
CUI: C0027439
Disease: Nasopharyngeal Neoplasms
183 0.801 0.321 9 22043927 intron variant A/G snp 0.30 0.800 2 2010 2016
Glaucoma
CUI: C0017601
Disease: Glaucoma
209 0.801 0.321 9 22043927 intron variant A/G snp 0.30 0.700 2 2011 2012
Calcification of coronary artery
CUI: C1611184
Disease: Calcification of coronary artery
3393 0.801 0.321 9 22043927 intron variant A/G snp 0.30 0.700 1 2012 2012
Anaplastic astrocytoma
CUI: C0334579
Disease: Anaplastic astrocytoma
6 0.801 0.321 9 22043927 intron variant A/G snp 0.30 0.010 1.000 1 2010 2010
Diabetes Mellitus, Non-Insulin-Dependent
1522 0.801 0.321 9 22043927 intron variant A/G snp 0.30 0.010 1.000 1 2008 2008
Nasopharyngeal carcinoma
CUI: C2931822
Disease: Nasopharyngeal carcinoma
60 0.801 0.321 9 22043927 intron variant A/G snp 0.30 0.010 1.000 1 2016 2016
Piebaldism
CUI: C0080024
Disease: Piebaldism
16 0.801 0.321 9 22043927 intron variant A/G snp 0.30 0.010 1.000 1 2015 2015