Gene: NQO2 ×
Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1143684
rs1143684
NQO2
4 0.882 0.160 6 3010156 missense variant C/T snv 0.79 0.84 0.010 1.000 1 2011 2011
dbSNP: rs201753355
rs201753355
NQO2 ; HTATSF1P2
2 0.925 0.120 6 3019647 missense variant G/A;C snv 2.0E-05 0.010 1.000 1 2011 2011