Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2155219 0.732 0.280 11 76588150 upstream gene variant G/T snv 0.52 14
rs7927894 0.742 0.320 11 76590272 upstream gene variant C/T snv 0.35 12
rs1837253 0.790 0.240 5 111066174 upstream gene variant T/C snv 0.72 10
rs479844 0.851 0.160 11 65784486 upstream gene variant A/G snv 0.44 6
rs17728338 0.851 0.160 5 151098757 downstream gene variant G/A snv 7.1E-02 4
rs4722404 0.851 0.120 7 3089155 intron variant T/C snv 0.40 4
rs4982958 0.851 0.200 14 24518659 intergenic variant C/T snv 0.50 4
rs7130588 0.882 0.200 11 76559639 regulatory region variant A/G snv 0.29 4
rs7936562 0.882 0.160 11 76567214 intergenic variant T/C snv 0.59 4
rs976078 0.882 0.120 13 82963398 intron variant A/C snv 0.15 4
rs12634229 0.882 0.120 3 112657461 intergenic variant T/C snv 0.15 3
rs17389644 0.925 0.120 4 122576542 intergenic variant G/A;T snv 3
rs174448 1.000 0.120 11 61872101 downstream gene variant G/A snv 0.61 3
rs712484 0.882 0.160 14 48081576 intergenic variant C/A snv 0.14 3
rs7124842 0.882 0.160 11 76600576 intergenic variant G/A;C;T snv 3
rs878860 0.882 0.120 11 7946812 intergenic variant C/T snv 0.35 3
rs112111458 0.925 0.120 2 70872975 intergenic variant A/G snv 0.16 2
rs12081541 0.925 0.160 1 152468890 intergenic variant T/C snv 8.9E-02 2
rs13132933 0.925 0.200 4 122089432 upstream gene variant T/C snv 0.22 2
rs1384974 0.925 0.120 3 177009491 downstream gene variant T/C snv 9.6E-02 2
rs1528473 0.925 0.120 15 55094545 downstream gene variant A/G snv 7.6E-02 2
rs2164983 0.925 0.120 19 8679120 downstream gene variant C/A;G snv 0.19 2
rs224108 0.925 0.120 10 62789851 intron variant T/C;G snv 0.21 2
rs5743399 0.925 0.120 8 6880123 intron variant G/A snv 0.31 2
rs6473227 0.925 0.120 8 80373657 intron variant C/A snv 0.54 2