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 0.763 0.320 12 68251271 intron variant C/G snv 0.18 0.020 1.000 2 2015 2016
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.763 0.320 12 68251271 intron variant C/G snv 0.18 0.020 1.000 2 2015 2016
Autoimmune thyroid disease (AITD)
CUI: C3840565
Disease: Autoimmune thyroid disease (AITD)
54 0.763 0.320 12 68251271 intron variant C/G snv 0.18 0.010 1.000 1 2017 2017
Colon Carcinoma
CUI: C0699790
Disease: Colon Carcinoma
275 0.763 0.320 12 68251271 intron variant C/G snv 0.18 0.010 1.000 1 2010 2010
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.763 0.320 12 68251271 intron variant C/G snv 0.18 0.010 1.000 1 2018 2018
Hashimoto Disease
CUI: C0677607
Disease: Hashimoto Disease
131 0.763 0.320 12 68251271 intron variant C/G snv 0.18 0.010 1.000 1 2017 2017
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.763 0.320 12 68251271 intron variant C/G snv 0.18 0.010 1.000 1 2018 2018
Infection caused by Helicobacter pylori
CUI: C0850666
Disease: Infection caused by Helicobacter pylori
56 0.763 0.320 12 68251271 intron variant C/G snv 0.18 0.010 1.000 1 2016 2016
Intestinal metaplasia
CUI: C0334037
Disease: Intestinal metaplasia
24 0.763 0.320 12 68251271 intron variant C/G snv 0.18 0.010 1.000 1 2016 2016
Malignant tumor of colon
CUI: C0007102
Disease: Malignant tumor of colon
688 0.763 0.320 12 68251271 intron variant C/G snv 0.18 0.010 1.000 1 2010 2010
Neoplasm Metastasis
CUI: C0027627
Disease: Neoplasm Metastasis
327 0.763 0.320 12 68251271 intron variant C/G snv 0.18 0.010 1.000 1 2015 2015
Precancerous Conditions
CUI: C0032927
Disease: Precancerous Conditions
18 0.763 0.320 12 68251271 intron variant C/G snv 0.18 0.010 1.000 1 2019 2019
Secondary Neoplasm
CUI: C2939419
Disease: Secondary Neoplasm
85 0.763 0.320 12 68251271 intron variant C/G snv 0.18 0.010 1.000 1 2015 2015
Thyroid associated opthalmopathies
CUI: C0339143
Disease: Thyroid associated opthalmopathies
49 0.763 0.320 12 68251271 intron variant C/G snv 0.18 0.010 1.000 1 2017 2017