rs12229892, PTPN11

N. diseases: 6
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.
Cleft Palate
CUI: C0008925
Disease: Cleft Palate
158 0.807 0.240 12 112485589 intron variant G/A snv 1.4E-02 0.700 1.000 1 2017 2017
Cleft upper lip
CUI: C0008924
Disease: Cleft upper lip
282 0.807 0.240 12 112485589 intron variant G/A snv 1.4E-02 0.700 1.000 1 2017 2017
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.807 0.240 12 112485589 intron variant G/A snv 1.4E-02 0.020 1.000 2 2013 2016
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.807 0.240 12 112485589 intron variant G/A snv 1.4E-02 0.020 1.000 2 2013 2016
Gastritis, Atrophic
CUI: C0017154
Disease: Gastritis, Atrophic
61 0.807 0.240 12 112485589 intron variant G/A snv 1.4E-02 0.010 1.000 1 2013 2013
Infection caused by Helicobacter pylori
CUI: C0850666
Disease: Infection caused by Helicobacter pylori
56 0.807 0.240 12 112485589 intron variant G/A snv 1.4E-02 0.010 1.000 1 2016 2016