Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 28
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 26
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 24
rs12980275 0.701 0.360 19 39241143 upstream gene variant A/G snv 0.36 23
rs635634 0.882 0.160 9 133279427 upstream gene variant T/A;C snv 22
rs651007 0.851 0.160 9 133278431 upstream gene variant T/A;C snv 22
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 21
rs247617 0.827 0.160 16 56956804 regulatory region variant C/A snv 0.29 20
rs478442 0.851 0.120 2 21176344 intergenic variant G/C;T snv 18
rs7703051 0.851 0.120 5 75329662 intron variant C/A snv 0.38 18
rs11065987 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 17
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 16
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 16
rs2954021 1.000 0.040 8 125469835 intron variant A/G snv 0.54 15
rs2954029 0.807 0.160 8 125478730 intron variant A/T snv 0.42 14
rs173539 0.882 0.080 16 56954132 intergenic variant C/T snv 0.33 11
rs9989419 0.882 0.120 16 56951227 regulatory region variant A/G snv 0.55 11
rs2001945 8 125465736 upstream gene variant G/A;C;T snv 10
rs602633 0.851 0.080 1 109278889 downstream gene variant T/G snv 0.63 10
rs649129 1.000 0.080 9 133278860 upstream gene variant T/C;G snv 10
rs2001844 0.882 0.040 8 125466503 upstream gene variant A/G snv 0.43 9
rs2954031 8 125479491 intron variant G/T snv 0.42 9
rs515135 0.807 0.160 2 21063185 intergenic variant T/C snv 0.73 9
rs9326246 0.925 0.040 11 116741017 intergenic variant C/G snv 0.93 9
rs12748152 1.000 0.120 1 26811902 upstream gene variant C/T snv 5.7E-02 8