rs10499563, STEAP1B

N. diseases: 7
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 0.807 0.120 7 22720869 intron variant T/C snv 0.21 0.020 1.000 2 2013 2017
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.807 0.120 7 22720869 intron variant T/C snv 0.21 0.020 1.000 2 2013 2017
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.807 0.120 7 22720869 intron variant T/C snv 0.21 0.010 1.000 1 2014 2014
Fatty Liver Disease
CUI: C4529962
Disease: Fatty Liver Disease
81 0.807 0.120 7 22720869 intron variant T/C snv 0.21 0.010 1.000 1 2016 2016
Infection caused by Helicobacter pylori
56 0.807 0.120 7 22720869 intron variant T/C snv 0.21 0.010 1.000 1 2017 2017
Inflammatory Bowel Diseases
CUI: C0021390
Disease: Inflammatory Bowel Diseases
605 0.807 0.120 7 22720869 intron variant T/C snv 0.21 0.010 1.000 1 2016 2016
Ulcerative Colitis
CUI: C0009324
Disease: Ulcerative Colitis
827 0.807 0.120 7 22720869 intron variant T/C snv 0.21 0.010 1.000 1 2014 2014