Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1079866 0.925 0.080 7 41430495 intergenic variant C/G snv 0.13 3
rs10825036 0.882 0.080 10 53506471 intergenic variant T/G snv 0.21 3
rs1154865 0.882 0.160 12 73596057 intergenic variant C/G snv 0.22 3
rs12422552 0.925 0.080 12 14260997 regulatory region variant G/C snv 0.30 3
rs1429142 0.882 0.080 4 147368237 intergenic variant T/C snv 0.34 3
rs166870 0.882 0.080 15 79777420 intergenic variant T/C;G snv 3
rs16886165 0.882 0.160 5 56727256 intergenic variant T/C;G snv 0.22 3
rs17094222 0.925 0.080 10 100635683 intergenic variant T/C snv 0.17 3
rs2380205 0.882 0.080 10 5844771 upstream gene variant C/T snv 0.47 3
rs2494251 0.925 0.080 1 159311361 downstream gene variant G/A;C snv 3
rs2823093 0.882 0.080 21 15148511 intergenic variant G/A snv 0.32 3
rs554219 0.925 0.080 11 69516874 regulatory region variant C/A;G;T snv 3
rs55834529 0.882 0.120 6 27104763 intergenic variant A/G snv 4.9E-02 3
rs6583267 0.882 0.120 3 195932298 intron variant A/G snv 3
rs6796502 0.882 0.080 3 46825376 downstream gene variant G/A;T snv 3
rs6913578 0.925 0.080 6 151628671 intergenic variant A/C;T snv 3
rs7107217 0.882 0.160 11 129603795 intron variant A/C;G snv 3
rs75915166 0.882 0.080 11 69564393 TF binding site variant C/A snv 3.9E-02 3
rs7821178 0.925 0.080 8 77181601 intergenic variant C/A;G;T snv 3
rs10043985 0.925 0.080 5 111065770 upstream gene variant A/C snv 5.2E-02 2
rs1034794 0.925 0.080 7 124801348 intergenic variant A/T snv 0.69 2
rs10472076 0.925 0.080 5 58888234 regulatory region variant T/A;C snv 2
rs10515083 0.925 0.080 17 54886696 intergenic variant T/A snv 0.46 2
rs10759243 0.925 0.080 9 107543834 upstream gene variant C/A;T snv 2
rs10902845 0.925 0.080 10 122923791 intergenic variant T/C snv 3.0E-02 2