Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 24
rs12229654 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 20
rs2954021 1.000 0.040 8 125469835 intron variant A/G snv 0.54 15
rs11065979 0.851 0.200 12 111621753 intergenic variant C/T snv 0.30 12
rs9989419 0.882 0.120 16 56951227 regulatory region variant A/G snv 0.55 11
rs12509595 1.000 0.080 4 80261400 intergenic variant T/C snv 0.23 10
rs4418728 10 93079967 downstream gene variant G/T snv 0.42 8
rs740746 10 114033028 intergenic variant G/A snv 0.70 8
rs1154988 3 136206349 upstream gene variant T/A snv 0.76 7
rs1531517 1.000 0.080 19 44738916 intergenic variant G/A snv 0.11 7
rs17451107 3 157079820 upstream gene variant T/C snv 0.38 7
rs11099097 4 80246155 intergenic variant C/T snv 0.30 6
rs112259268 17 43797377 downstream gene variant C/A snv 1.9E-02 6
rs13125101 4 80253438 TF binding site variant G/A snv 0.24 6
rs13149993 4 80237391 regulatory region variant G/A;C snv 6
rs1495743 8 18415790 intergenic variant G/A;C snv 6
rs2643826 3 27521497 upstream gene variant C/T snv 0.56 6
rs35444 12 115114632 intergenic variant A/G snv 0.38 6
rs9292468 5 32818967 intergenic variant T/A;C snv 6
rs10184428 2 164155317 intron variant C/A;G snv 5
rs11513729 1.000 0.080 12 111835695 downstream gene variant C/T snv 0.29 5
rs13209747 6 126794309 intron variant C/G;T snv 0.36 5
rs2013002 12 111762346 intron variant T/A;C snv 5
rs35225200 1.000 0.040 4 102225731 intergenic variant A/C snv 5.4E-02 5
rs35441 12 115115310 intergenic variant C/T snv 0.40 5