Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2036527 0.851 0.080 15 78559273 regulatory region variant G/A snv 0.29 12
rs2857595 0.827 0.320 6 31600692 intergenic variant G/A snv 0.27 9
rs13141641 1.000 0.040 4 144585304 intron variant T/C snv 0.32 8
rs2145272 20 6645571 intergenic variant G/A;T snv 8
rs13118928 0.925 0.040 4 144565237 intron variant A/G snv 0.33 7
rs7655625 1.000 0.040 4 144564763 intron variant T/C;G snv 7
rs9368649 0.925 0.040 6 30971106 intergenic variant A/G snv 0.10 7
rs1980057 1.000 0.040 4 144564586 intron variant C/T snv 0.31 6
rs979012 1.000 0.080 20 6642727 intergenic variant T/C snv 0.67 6
rs1512288 1.000 0.040 4 144570129 intron variant G/A snv 0.42 5
rs1541374 4 105127203 intergenic variant T/A;G snv 5
rs35755165 0.882 0.080 19 40840084 intron variant A/C;G snv 5
rs554543329 1.000 6 30971106 intergenic variant A/G snv 5
rs6817273 1.000 0.040 4 144570851 intron variant T/A;C snv 0.33 5
rs12198986 6 7719826 regulatory region variant G/A snv 0.37 4
rs12477314 2 238955452 regulatory region variant C/G;T snv 4
rs1394371 0.925 0.080 15 78432127 intergenic variant C/T snv 0.22 4
rs1496255 4 120683279 downstream gene variant G/A;T snv 4
rs2316205 19 40840863 non coding transcript exon variant T/C snv 0.40 4
rs4887053 0.925 0.080 15 78420357 regulatory region variant A/C;T snv 4
rs6537296 4 144566782 intron variant A/G snv 0.37 4
rs10751226 11 73601207 upstream gene variant C/G;T snv 3
rs1102077 6 139950220 intron variant A/C snv 0.21 3
rs11176001 12 66015587 regulatory region variant C/A snv 9.6E-02 3
rs113029345 19 40864271 intron variant T/C snv 3