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.
Allergic Reaction
CUI: C1527304
Disease: Allergic Reaction
1019 0.776 0.240 1 24925432 intron variant A/T snv 0.42 0.700 1.000 1 2017 2017
Eczema
CUI: C0013595
Disease: Eczema
368 0.776 0.240 1 24925432 intron variant A/T snv 0.42 0.700 1.000 1 2019 2019
Asphyxia Neonatorum
CUI: C0004045
Disease: Asphyxia Neonatorum
5 0.776 0.240 1 24925432 intron variant A/T snv 0.42 0.010 1.000 1 2019 2019
Bladder Neoplasm
CUI: C0005695
Disease: Bladder Neoplasm
281 0.776 0.240 1 24925432 intron variant A/T snv 0.42 0.010 1.000 1 2008 2008
Carcinoma of bladder
CUI: C0699885
Disease: Carcinoma of bladder
309 0.776 0.240 1 24925432 intron variant A/T snv 0.42 0.010 1.000 1 2008 2008
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.776 0.240 1 24925432 intron variant A/T snv 0.42 0.010 1 2015 2015
Gastritis, Atrophic
CUI: C0017154
Disease: Gastritis, Atrophic
61 0.776 0.240 1 24925432 intron variant A/T snv 0.42 0.010 1.000 1 2009 2009
Helicobacter pylori (H. pylori) infection in conditions classified elsewhere and of unspecified site
CUI: C0374997
Disease: Helicobacter pylori (H. pylori) infection in conditions classified elsewhere and of unspecified site
24 0.776 0.240 1 24925432 intron variant A/T snv 0.42 0.010 1.000 1 2009 2009
Malignant neoplasm of urinary bladder
CUI: C0005684
Disease: Malignant neoplasm of urinary bladder
316 0.776 0.240 1 24925432 intron variant A/T snv 0.42 0.010 1.000 1 2008 2008