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: rs710521
rs710521
4 0.851 0.200 3 189928144 intergenic variant T/C snv 0.24 0.740 1.000 8 2008 2018
dbSNP: rs1495741
rs1495741
9 0.827 0.240 8 18415371 regulatory region variant G/A snv 0.71 0.720 1.000 4 2010 2016
dbSNP: rs833052
rs833052
5 0.827 0.160 6 43755598 intergenic variant A/C snv 0.88 0.040 1.000 4 2007 2019
dbSNP: rs1014971
rs1014971
3 0.882 0.120 22 38936618 regulatory region variant C/T snv 0.55 0.720 1.000 3 2010 2016
dbSNP: rs8102137
rs8102137
3 0.882 0.120 19 29805946 regulatory region variant T/C snv 0.24 0.720 1.000 3 2010 2014
dbSNP: rs10234749
rs10234749
3 0.882 0.120 7 152690784 regulatory region variant T/C;G snv 0.010 1.000 1 2007 2007
dbSNP: rs1024611
rs1024611
63 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 0.010 1.000 1 2012 2012
dbSNP: rs10811474
rs10811474
11 0.742 0.240 9 21114238 intergenic variant A/G snv 0.44 0.010 1.000 1 2014 2014
dbSNP: rs1109324
rs1109324
5 0.827 0.160 6 43762018 intergenic variant G/T snv 0.15 0.010 1.000 1 2007 2007
dbSNP: rs1547651
rs1547651
4 0.851 0.200 6 43762907 regulatory region variant A/T snv 0.15 0.010 1.000 1 2007 2007
dbSNP: rs1937920
rs1937920
2 0.925 0.120 10 5119763 downstream gene variant A/G snv 0.28 0.010 1.000 1 2016 2016
dbSNP: rs2204008
rs2204008
1 1.000 0.120 12 38045401 intergenic variant C/A;T snv 0.700 1.000 1 2014 2014
dbSNP: rs2505568
rs2505568
4 0.851 0.160 10 36522408 non coding transcript exon variant T/A snv 0.56 0.010 1.000 1 2014 2014
dbSNP: rs2764736
rs2764736
4 0.851 0.160 9 25067733 intergenic variant T/C snv 2.4E-02 0.010 1.000 1 2014 2014
dbSNP: rs398652
rs398652
10 0.752 0.240 14 56058851 intergenic variant G/A snv 0.24 0.010 1.000 1 2011 2011
dbSNP: rs62185668
rs62185668
3 0.925 0.120 20 10981287 intron variant C/A snv 0.19 0.710 1.000 1 2014 2014
dbSNP: rs6464268
rs6464268
3 0.882 0.120 7 152684065 intergenic variant A/G snv 0.23 0.010 1.000 1 2007 2007
dbSNP: rs715021
rs715021
3 0.882 0.120 2 221196620 intergenic variant C/G snv 0.26 0.010 1.000 1 2009 2009
dbSNP: rs874945
rs874945
14 0.732 0.240 12 53961667 upstream gene variant C/T snv 0.38 0.010 1.000 1 2018 2018
dbSNP: rs921142
rs921142
3 0.882 0.120 8 41311757 upstream gene variant T/C snv 0.31 0.010 < 0.001 1 2013 2013
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 2002 2002
dbSNP: rs4986826
rs4986826
AHR
3 0.882 0.120 7 17339533 missense variant G/A snv 7.8E-03 2.2E-02 0.010 1.000 1 2002 2002
dbSNP: rs12529
rs12529
10 0.776 0.280 10 5094459 missense variant C/G snv 0.50 0.45 0.020 1.000 2 2011 2016
dbSNP: rs1130214
rs1130214
12 0.742 0.280 14 104793397 5 prime UTR variant C/A snv 0.31 0.010 1.000 1 2018 2018
dbSNP: rs1130233
rs1130233
13 0.742 0.480 14 104773557 synonymous variant C/T snv 0.30 0.23 0.010 1.000 1 2018 2018