Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs635634 0.882 0.160 9 133279427 upstream gene variant T/A;C snv 22
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 21
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 20
rs651007 0.851 0.160 9 133278431 upstream gene variant T/A;C snv 20
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 18
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 17
rs12229654 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 14
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 12
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 11
rs649129 1.000 0.080 9 133278860 upstream gene variant T/C;G snv 10
rs9989419 0.882 0.120 16 56951227 regulatory region variant A/G snv 0.55 10
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 9
rs17482753 1.000 0.080 8 19975135 regulatory region variant G/T snv 8.8E-02 8
rs2820443 0.882 0.120 1 219580167 regulatory region variant T/C snv 0.23 8
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 8
rs6905288 0.882 0.120 6 43791136 downstream gene variant G/A snv 0.56 8
rs12970134 0.790 0.280 18 60217517 intergenic variant G/A snv 0.21 7
rs2943641 0.763 0.160 2 226229029 intergenic variant T/C snv 0.67 7
rs71597855 0.807 0.240 4 53790270 intron variant G/A snv 2.5E-02 7
rs727428 0.882 0.200 17 7634474 downstream gene variant T/C snv 0.55 7
rs17411031 0.925 0.120 8 19994799 regulatory region variant C/G snv 0.25 6
rs2867125 0.925 0.120 2 622827 intergenic variant T/A;C snv 0.85 6
rs8089364 0.925 0.120 18 60191596 upstream gene variant T/C snv 0.21 6
rs10184004 1.000 0.080 2 164651879 downstream gene variant C/T snv 0.48 5
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 5