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: 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: 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: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 1 2011 2011