Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12509595 1.000 0.080 4 80261400 intergenic variant T/C snv 0.23 10
rs2472297 0.882 0.160 15 74735539 intergenic variant C/T snv 0.16 9
rs4410790 0.882 0.160 7 17244953 intron variant T/C snv 0.54 9
rs784257 1.000 0.080 18 55729968 intron variant T/A;C snv 4
rs17046344 2 54796463 intron variant G/A snv 0.11 3
rs588321 11 1875727 intron variant G/C;T snv 3
rs36096257 2 121281207 missense variant G/A snv 6.8E-03 2.9E-03 3
rs7215775 17 61406955 non coding transcript exon variant A/G snv 0.68 2
rs7495833 15 53651121 intron variant C/A snv 0.37 2
rs12037987 1 112500200 intron variant T/C snv 8.6E-02 2
rs1290083 15 50858717 intron variant T/A;C snv 1
rs12944041 17 8169779 downstream gene variant G/A snv 0.42 1
rs13143189 4 3755653 downstream gene variant G/A snv 0.36 1
rs254023 5 104619660 intron variant T/C snv 0.43 1
rs4973766 3 27372075 intron variant C/T snv 0.38 1
rs6647951 X 76165707 intergenic variant C/T snv 2.2E-02 1
rs72704791 5 547781 intergenic variant A/G snv 0.14 1
rs6467447 7 132840387 intron variant C/T snv 0.69 1
rs12465752 2 121355564 intron variant C/T snv 0.12 1
rs10854166 19 18542034 5 prime UTR variant A/G snv 0.46 0.37 1
rs929250 7 27205482 non coding transcript exon variant G/T snv 0.93 1
rs1275980 2 26694101 intron variant C/T snv 0.48 1
rs5912570 X 78218174 intergenic variant C/T snv 0.45 1
rs61375854 6 54681503 intergenic variant T/G snv 0.40 1
rs118070237 16 56795510 intron variant T/C snv 4.7E-04 1