Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12826786 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 26
rs13361189 0.752 0.240 5 150843825 upstream gene variant T/C snv 0.21 13
rs398652 0.752 0.240 14 56058851 intergenic variant G/A snv 0.24 10
rs4635969 0.827 0.160 5 1308437 downstream gene variant G/A;T snv 7
rs2252586 0.882 0.040 7 54911231 intergenic variant C/T snv 0.27 5
rs75061358 0.882 0.040 7 54848587 intergenic variant T/C;G snv 4
rs13332653 0.882 0.040 16 24578078 intergenic variant T/G snv 0.11 3
rs9933544 0.882 0.040 16 24576962 downstream gene variant A/C snv 0.29 3
rs12088062 1.000 0.040 1 244811284 intergenic variant C/T snv 0.20 2
rs1409785 1.000 0.040 1 74782438 intergenic variant G/A snv 0.65 2
rs16838813 1.000 0.040 1 4364085 intergenic variant G/A;T snv 0.11 2
rs11216943 1.000 0.040 11 118685689 downstream gene variant G/A snv 0.20 1
rs147061479 1.000 0.040 8 65264756 intergenic variant C/T snv 1.9E-02 1
rs6554759 1.000 0.040 5 1316987 downstream gene variant G/A snv 0.85 1
rs7300686 1.000 0.040 12 128062664 intron variant C/A;T snv 1
rs9841110 1.000 0.040 3 49455048 regulatory region variant C/G snv 0.28 1
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs17110757
ACOT11
1.000 0.040 1 54584133 intron variant G/A snv 0.20 2
rs12615793
ACYP2
0.851 0.280 2 54248777 intron variant G/A;T snv 4
rs843720
ACYP2 ; LOC105374610
0.752 0.280 2 54283523 intron variant T/G snv 0.52 10
rs201963
ADAM18
1.000 0.040 8 39721376 intron variant A/C snv 1
rs2066853
AHR
0.653 0.600 7 17339486 missense variant G/A snv 0.15 0.22 34
rs2158041
AHR
0.807 0.160 7 17328796 intron variant T/C snv 0.81 6
rs2239647
AKAP6
0.851 0.080 14 32823537 synonymous variant A/C snv 0.60 0.65 7
rs10131032
AKAP6
1.000 0.040 14 32780875 intron variant G/A snv 9.3E-02 2