rs158572, ERCC8;NDUFAF2

N. diseases: 4
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.
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.851 0.120 5 60943616 intron variant G/A snv 0.63 0.030 1.000 3 2015 2018
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.851 0.120 5 60943616 intron variant G/A snv 0.63 0.030 1.000 3 2015 2018
Gastritis, Atrophic
CUI: C0017154
Disease: Gastritis, Atrophic
61 0.851 0.120 5 60943616 intron variant G/A snv 0.63 0.020 1.000 2 2015 2017
Infection caused by Helicobacter pylori
CUI: C0850666
Disease: Infection caused by Helicobacter pylori
56 0.851 0.120 5 60943616 intron variant G/A snv 0.63 0.010 1.000 1 2018 2018