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: rs1042028
rs1042028
SULT1A1
30 0.658 0.440 16 28606193 missense variant C/T snv 0.22 0.30 0.010 1.000 1 2015 2015
dbSNP: rs1131341
rs1131341
NQO1
4 0.925 0.160 16 69714966 missense variant G/A;C snv 3.2E-02 2.6E-02 0.010 1.000 1 2005 2005
dbSNP: rs1233753551
rs1233753551
CYP1B1 ; CYP1B1-AS1
4 0.851 0.160 2 38074751 missense variant C/T snv 7.0E-06 0.010 1.000 1 2015 2015
dbSNP: rs1258159645
rs1258159645
NQO1
37 0.630 0.600 16 69711128 missense variant G/A snv 7.0E-06 0.010 1.000 1 2005 2005
dbSNP: rs1800566
rs1800566
NQO1
59 0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 0.010 1.000 1 2005 2005
dbSNP: rs587781288
rs587781288
TP53
16 0.732 0.440 17 7675190 missense variant C/A;T snv 0.010 1.000 1 1998 1998
dbSNP: rs854560
rs854560
PON1
113 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.010 1.000 1 2012 2012
dbSNP: rs9282861
rs9282861
SULT1A1
31 0.658 0.440 16 28606193 missense variant C/T snv 0.010 1.000 1 2015 2015