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: rs13009079
rs13009079
3 0.882 0.080 2 174396420 intron variant T/C snv 0.26 0.020 1.000 2 2014 2016
dbSNP: rs156641
rs156641
3 0.882 0.080 19 48128151 intron variant C/T snv 0.29 0.020 0.500 2 2008 2015
dbSNP: rs20579
rs20579
3 0.882 0.080 19 48165573 5 prime UTR variant G/A;C snv 0.13 0.020 0.500 2 2008 2015
dbSNP: rs3730931
rs3730931
3 0.882 0.080 19 48143984 intron variant T/C snv 0.12 0.15 0.020 0.500 2 2008 2015
dbSNP: rs439132
rs439132
3 0.882 0.080 19 48165657 intron variant T/C snv 5.6E-02 9.6E-02 0.020 0.500 2 2008 2015
dbSNP: rs763317
rs763317
3 0.882 0.080 7 55027504 intron variant A/G snv 0.59 0.020 1.000 2 2009 2015
dbSNP: rs7811989
rs7811989
AHR
3 0.882 0.080 7 17331739 intron variant A/G snv 0.76 0.020 1.000 2 2009 2018
dbSNP: rs1002481
rs1002481
3 0.882 0.080 6 111390819 intron variant T/A;G snv 0.010 1.000 1 2013 2013
dbSNP: rs10040363
rs10040363
3 0.882 0.080 5 83177826 intron variant A/G snv 0.50 0.010 1.000 1 2011 2011
dbSNP: rs10053847
rs10053847
3 0.882 0.080 5 35878038 3 prime UTR variant G/A snv 0.13 0.010 1.000 1 2019 2019
dbSNP: rs10054203
rs10054203
3 0.882 0.080 5 1279849 intron variant G/A;C;T snv 0.010 1.000 1 2019 2019
dbSNP: rs1014264982
rs1014264982
3 0.882 0.080 19 3577038 missense variant G/A;C snv 6.8E-06 7.0E-06 0.010 1.000 1 2014 2014
dbSNP: rs10187911
rs10187911
3 0.882 0.080 2 50420809 intron variant C/A;G;T snv 0.010 1.000 1 2013 2013
dbSNP: rs10244817
rs10244817
3 0.882 0.080 7 124827416 intron variant T/C snv 0.22 0.010 1.000 1 2009 2009
dbSNP: rs10412613
rs10412613
3 0.882 0.080 19 52209575 intron variant G/A snv 0.63 0.010 1.000 1 2017 2017
dbSNP: rs1043973338
rs1043973338
3 0.882 0.080 2 112830483 missense variant A/C snv 0.010 1.000 1 2007 2007
dbSNP: rs10487372
rs10487372
3 0.882 0.080 7 117560845 intron variant C/T snv 0.13 0.010 1.000 1 2010 2010
dbSNP: rs1049337
rs1049337
3 0.882 0.080 7 116560533 3 prime UTR variant C/T snv 0.25 0.010 1.000 1 2017 2017
dbSNP: rs10508266
rs10508266
3 0.882 0.080 10 3797822 intergenic variant G/A;T snv 0.010 1.000 1 2007 2007
dbSNP: rs10512948
rs10512948
3 0.882 0.080 5 8233238 intron variant T/C snv 0.15 0.010 1.000 1 2013 2013
dbSNP: rs1053566
rs1053566
3 0.882 0.080 19 7911079 missense variant C/T snv 0.010 1.000 1 2016 2016
dbSNP: rs1057519984
rs1057519984
3 0.882 0.080 17 7673777 missense variant G/C;T snv 0.010 1.000 1 2012 2012
dbSNP: rs1060503291
rs1060503291
APC
3 0.882 0.080 5 112835135 missense variant C/T snv 0.010 1.000 1 2004 2004
dbSNP: rs10750417
rs10750417
3 0.882 0.080 11 129612280 non coding transcript exon variant A/G;T snv 0.010 < 0.001 1 2018 2018
dbSNP: rs10853100
rs10853100
3 0.882 0.080 17 48525070 downstream gene variant T/C snv 0.41 0.010 1.000 1 2018 2018