Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs56211063 1.000 0.080 9 114823617 regulatory region variant G/C snv 4.3E-02 1
rs564614982 1.000 0.080 17 46256922 downstream gene variant C/G;T snv 1
rs5757618 1.000 0.080 22 39328546 regulatory region variant A/T snv 0.19 1
rs6020940 1.000 0.080 20 51058312 intergenic variant G/A snv 0.82 1
rs6020957 1.000 0.080 20 51071098 TF binding site variant T/A;C snv 1
rs6478394 1.000 0.080 9 119074396 regulatory region variant A/G snv 0.32 1
rs6555969 1.000 0.080 5 171701460 regulatory region variant T/C snv 0.73 1
rs6871748 1.000 0.080 5 35885880 intergenic variant T/C snv 0.21 1
rs7117261 1.000 0.080 11 118870448 regulatory region variant T/A;C snv 0.80 1
rs7119044 1.000 0.080 11 118867589 intergenic variant G/C;T snv 1
rs7214306 1.000 0.080 17 71925130 intergenic variant T/C snv 0.33 1
rs7664828 1.000 0.080 4 102630219 downstream gene variant C/T snv 0.55 1
rs7677509 1.000 0.080 4 102628849 downstream gene variant T/C snv 0.55 1
rs7699231 1.000 0.080 4 102628918 downstream gene variant A/G snv 0.55 1
rs7699678 1.000 0.080 4 102628939 downstream gene variant G/A snv 0.55 1
rs77871618 1.000 0.080 11 118862915 intergenic variant C/T snv 6.6E-03 1
rs80065107 1.000 0.080 11 118812058 regulatory region variant T/C snv 1
rs8079498 1.000 0.080 17 71923311 intergenic variant T/C snv 0.32 1
rs911015 1.000 0.080 20 51073634 intergenic variant A/G;T snv 1
rs911020 1.000 0.080 20 51055409 intergenic variant T/C snv 0.94 1
rs974448 1.000 0.080 2 222140595 intergenic variant A/G snv 0.16 1
rs9858909 1.000 0.080 3 88329198 intergenic variant A/G snv 0.54 1
rs9910826 1.000 0.080 17 39879395 downstream gene variant A/G;T snv 1
rs2287618
ABCB11
1.000 0.080 2 168986299 intron variant T/C snv 0.69 0.73 1
rs1149222
ABCB4
1.000 0.080 7 87444459 intron variant G/T snv 0.67 1