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: 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