Source: BEFREE

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: rs1143684
rs1143684
NQO2
0.882 0.160 6 3010156 missense variant C/T snv 0.79 0.84
CUI: C0235974
Disease: Pancreatic carcinoma
Pancreatic carcinoma 		0.010 1.000 1 2011 2011
dbSNP: rs201753355
rs201753355
NQO2 ; HTATSF1P2
0.925 0.120 6 3019647 missense variant G/A;C snv 2.0E-05
CUI: C0235974
Disease: Pancreatic carcinoma
Pancreatic carcinoma 		0.010 1.000 1 2011 2011