Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1893217
rs1893217
PTPN2
0.742 0.440 18 12809341 intron variant A/G snv 0.12
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.850 1.000 3 2008 2016
dbSNP: rs1893217
rs1893217
PTPN2
0.742 0.440 18 12809341 intron variant A/G snv 0.12
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		0.830 0.667 2 2009 2019
dbSNP: rs1893217
rs1893217
PTPN2
0.742 0.440 18 12809341 intron variant A/G snv 0.12
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		0.810 1.000 1 2012 2016
dbSNP: rs1893217
rs1893217
PTPN2
0.742 0.440 18 12809341 intron variant A/G snv 0.12
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases 		0.810 1.000 1 2011 2019
dbSNP: rs11875687
rs11875687
PTPN2
1.000 0.080 18 12843138 intron variant T/C snv 0.17
CUI: C0007570
Disease: Celiac Disease
Celiac Disease 		0.800 1.000 2 2011 2012
dbSNP: rs1893217
rs1893217
PTPN2
0.742 0.440 18 12809341 intron variant A/G snv 0.12
CUI: C0007570
Disease: Celiac Disease
Celiac Disease 		0.800 1.000 1 2010 2010
dbSNP: rs1893217
rs1893217
PTPN2
0.742 0.440 18 12809341 intron variant A/G snv 0.12
CUI: C0021053
Disease: Immune System Diseases
Immune System Diseases 		0.800 1.000 1 2011 2011
dbSNP: rs2847281
rs2847281
PTPN2
1.000 0.040 18 12821594 intron variant A/G snv 0.32
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement 		0.800 1.000 1 2011 2011
dbSNP: rs2847281
rs2847281
PTPN2
1.000 0.040 18 12821594 intron variant A/G snv 0.32
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms 		0.800 1.000 1 2012 2012
dbSNP: rs2847297
rs2847297
PTPN2
0.827 0.200 18 12797695 intron variant A/G snv 0.40
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.800 1.000 1 2012 2015
dbSNP: rs8083786
rs8083786
PTPN2
1.000 0.120 18 12881362 intron variant A/G snv 0.27
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.800 1.000 1 2014 2019
dbSNP: rs16939895
rs16939895
PTPN2
1.000 0.120 18 12821904 intron variant G/A snv 0.17
CUI: C3495559
Disease: Juvenile arthritis
Juvenile arthritis 		0.700 1.000 1 2012 2012
dbSNP: rs1893217
rs1893217
PTPN2
0.742 0.440 18 12809341 intron variant A/G snv 0.12
CUI: C0004096
Disease: Asthma
Asthma 		0.700 1.000 1 2011 2011
dbSNP: rs1893217
rs1893217
PTPN2
0.742 0.440 18 12809341 intron variant A/G snv 0.12
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.700 1.000 1 2011 2011
dbSNP: rs657555
rs657555
PTPN2
0.925 0.080 18 12847137 intron variant C/A;T snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 1 2011 2011
dbSNP: rs657555
rs657555
PTPN2
0.925 0.080 18 12847137 intron variant C/A;T snv
CUI: C0021053
Disease: Immune System Diseases
Immune System Diseases 		0.700 1.000 1 2011 2011
dbSNP: rs657555
rs657555
PTPN2
0.925 0.080 18 12847137 intron variant C/A;T snv
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases 		0.700 1.000 1 2011 2011
dbSNP: rs7234029
rs7234029
PTPN2
0.807 0.320 18 12877061 intron variant A/G snv 0.27
CUI: C3495559
Disease: Juvenile arthritis
Juvenile arthritis 		0.700 1.000 1 2012 2012