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: rs523349
rs523349
21 0.689 0.440 2 31580636 missense variant G/A;C;T snv 0.66; 4.9E-06 0.020 1.000 2 2003 2014
dbSNP: rs1110061
rs1110061
7 0.807 0.200 9 124500523 missense variant C/A;G snv 4.3E-06; 0.10 0.010 1.000 1 2005 2005
dbSNP: rs121434250
rs121434250
7 0.790 0.200 2 31529419 missense variant C/G;T snv 1.4E-04 1.5E-04 0.010 1.000 1 2010 2010
dbSNP: rs121912530
rs121912530
4 0.851 0.160 2 48687923 missense variant A/T snv 7.0E-06 0.010 1.000 1 2002 2002
dbSNP: rs1311014616
rs1311014616
2 0.925 0.040 2 31580733 missense variant C/G snv 8.4E-06 0.010 1.000 1 2009 2009
dbSNP: rs2066479
rs2066479
7 0.790 0.160 9 96235528 missense variant C/A;G;T snv 7.2E-02 0.010 1.000 1 2017 2017
dbSNP: rs2066853
rs2066853
AHR
34 0.653 0.600 7 17339486 missense variant G/A snv 0.15 0.22 0.010 1.000 1 2005 2005
dbSNP: rs2292596
rs2292596
7 0.827 0.240 5 422840 missense variant C/G;T snv 0.38; 4.0E-06 0.010 1.000 1 2005 2005
dbSNP: rs371701248
rs371701248
3 0.882 0.160 9 124491156 missense variant C/T snv 1.3E-04 5.6E-05 0.010 1.000 1 2007 2007
dbSNP: rs554416372
rs554416372
WT1
5 0.827 0.160 11 32396397 missense variant C/A;G;T snv 2.0E-05; 8.0E-06; 9.6E-05 0.010 1.000 1 2018 2018
dbSNP: rs9332964
rs9332964
10 0.763 0.240 2 31529325 missense variant C/T snv 4.7E-04 1.6E-04 0.010 1.000 1 2003 2003