rs1893217, PTPN2

N. diseases: 10
Source: GWASCAT ×
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.
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
616 0.742 0.440 18 12809341 intron variant A/G snv 0.12 0.850 1.000 2 2008 2016
Diabetes Mellitus, Insulin-Dependent
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
198 0.742 0.440 18 12809341 intron variant A/G snv 0.12 0.830 0.667 2 2009 2019
Autoimmune Diseases
CUI: C0004364
Disease: Autoimmune Diseases
145 0.742 0.440 18 12809341 intron variant A/G snv 0.12 0.810 1.000 2 2011 2019
Inflammatory Bowel Diseases
CUI: C0021390
Disease: Inflammatory Bowel Diseases
354 0.742 0.440 18 12809341 intron variant A/G snv 0.12 0.810 1.000 2 2012 2016
Celiac Disease
CUI: C0007570
Disease: Celiac Disease
178 0.742 0.440 18 12809341 intron variant A/G snv 0.12 0.800 1.000 1 2010 2010
Immune System Diseases
CUI: C0021053
Disease: Immune System Diseases
17 0.742 0.440 18 12809341 intron variant A/G snv 0.12 0.800 1.000 1 2011 2011
Ulcerative Colitis
CUI: C0009324
Disease: Ulcerative Colitis
464 0.742 0.440 18 12809341 intron variant A/G snv 0.12 0.720 1.000 1 2014 2016
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1
CUI: C4014795
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1
130 0.742 0.440 18 12809341 intron variant A/G snv 0.12 0.700 1.000 1 2019 2019
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2
CUI: C4310768
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2
130 0.742 0.440 18 12809341 intron variant A/G snv 0.12 0.700 1.000 1 2019 2019
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6
CUI: C3150797
Disease: AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6
130 0.742 0.440 18 12809341 intron variant A/G snv 0.12 0.700 1.000 1 2019 2019