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: rs2252586
rs2252586 		5 0.882 0.040 7 54911231 intergenic variant C/T snv 0.27 0.860 0.833 6 2011 2017
dbSNP: rs75061358
rs75061358 		4 0.882 0.040 7 54848587 intergenic variant T/C;G snv 0.700 1.000 3 2015 2018
dbSNP: rs11216943
rs11216943 		1 1.000 0.040 11 118685689 downstream gene variant G/A snv 0.20 0.700 1.000 1 2011 2011
dbSNP: rs12088062
rs12088062 		2 1.000 0.040 1 244811284 intergenic variant C/T snv 0.20 0.700 1.000 1 2009 2009
dbSNP: rs12826786
rs12826786 		26 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 0.010 < 0.001 1 2017 2017
dbSNP: rs13332653
rs13332653 		3 0.882 0.040 16 24578078 intergenic variant T/G snv 0.11 0.010 1.000 1 2014 2014
dbSNP: rs13361189
rs13361189 		13 0.752 0.240 5 150843825 upstream gene variant T/C snv 0.21 0.010 1.000 1 2014 2014
dbSNP: rs1409785
rs1409785 		2 1.000 0.040 1 74782438 intergenic variant G/A snv 0.65 0.700 1.000 1 2009 2009
dbSNP: rs147061479
rs147061479 		1 1.000 0.040 8 65264756 intergenic variant C/T snv 1.9E-02 0.010 1.000 1 2016 2016
dbSNP: rs16838813
rs16838813 		2 1.000 0.040 1 4364085 intergenic variant G/A;T snv 0.11 0.700 1.000 1 2009 2009
dbSNP: rs398652
rs398652 		10 0.752 0.240 14 56058851 intergenic variant G/A snv 0.24 0.010 1.000 1 2014 2014
dbSNP: rs4635969
rs4635969 		7 0.827 0.160 5 1308437 downstream gene variant G/A;T snv 0.010 1.000 1 2012 2012
dbSNP: rs6554759
rs6554759 		1 1.000 0.040 5 1316987 downstream gene variant G/A snv 0.85 0.010 1.000 1 2012 2012
dbSNP: rs7300686
rs7300686 		1 1.000 0.040 12 128062664 intron variant C/A;T snv 0.700 1.000 1 2009 2009
dbSNP: rs9841110
rs9841110 		1 1.000 0.040 3 49455048 regulatory region variant C/G snv 0.28 0.700 1.000 1 2018 2018
dbSNP: rs9933544
rs9933544 		3 0.882 0.040 16 24576962 downstream gene variant A/C snv 0.29 0.010 1.000 1 2014 2014
dbSNP: rs1045642
rs1045642
ABCB1
214 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.010 < 0.001 1 2005 2005
dbSNP: rs17110757
rs17110757
ACOT11
2 1.000 0.040 1 54584133 intron variant G/A snv 0.20 0.700 1.000 1 2009 2009
dbSNP: rs12615793
rs12615793
ACYP2
4 0.851 0.280 2 54248777 intron variant G/A;T snv 0.010 1.000 1 2017 2017
dbSNP: rs843720
rs843720
ACYP2 ; LOC105374610
10 0.752 0.280 2 54283523 intron variant T/G snv 0.52 0.010 1.000 1 2017 2017
dbSNP: rs201963
rs201963
ADAM18
1 1.000 0.040 8 39721376 intron variant A/C snv 0.010 1.000 1 2016 2016
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 2012 2012
dbSNP: rs2158041
rs2158041
AHR
6 0.807 0.160 7 17328796 intron variant T/C snv 0.81 0.010 1.000 1 2012 2012
dbSNP: rs10131032
rs10131032
AKAP6
2 1.000 0.040 14 32780875 intron variant G/A snv 9.3E-02 0.700 1.000 1 2017 2017
dbSNP: rs2239647
rs2239647
AKAP6
7 0.851 0.080 14 32823537 synonymous variant A/C snv 0.60 0.65 0.010 1.000 1 2019 2019