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.
Leukemia, Myelocytic, Acute
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
6892 0.807 0.280 12 10119994 intron variant G/C snv 0.42 0.020 1.000 2 2016 2019
Incontinentia Pigmenti Achromians
CUI: C0022283
Disease: Incontinentia Pigmenti Achromians
10 0.807 0.280 12 10119994 intron variant G/C snv 0.42 0.010 1.000 1 2012 2012
Intrinsic Factor Deficiency
CUI: C1394891
Disease: Intrinsic Factor Deficiency
6 0.807 0.280 12 10119994 intron variant G/C snv 0.42 0.010 1.000 1 2019 2019
Invasive Fungal Infections
CUI: C1262313
Disease: Invasive Fungal Infections
5 0.807 0.280 12 10119994 intron variant G/C snv 0.42 0.010 1.000 1 2019 2019
Invasive Pulmonary Aspergillosis
CUI: C0276653
Disease: Invasive Pulmonary Aspergillosis
3 0.807 0.280 12 10119994 intron variant G/C snv 0.42 0.010 1.000 1 2019 2019
Mycoses
CUI: C0026946
Disease: Mycoses
2 0.807 0.280 12 10119994 intron variant G/C snv 0.42 0.010 1.000 1 2019 2019
Oropharyngeal candidiasis
CUI: C0919659
Disease: Oropharyngeal candidiasis
3 0.807 0.280 12 10119994 intron variant G/C snv 0.42 0.010 1.000 1 2019 2019
Pneumonia
CUI: C0032285
Disease: Pneumonia
33 0.807 0.280 12 10119994 intron variant G/C snv 0.42 0.010 1.000 1 2016 2016