Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2965667 0.776 0.080 12 17291799 intergenic variant A/T snv 0.96 10
rs3024505 0.790 0.320 1 206766559 upstream gene variant G/A snv 0.11 10
rs3133285 0.776 0.080 8 116617172 intergenic variant G/C snv 0.19 10
rs34405347 0.776 0.080 9 98917470 regulatory region variant T/C;G snv 10
rs34797592 0.776 0.080 19 16306387 intron variant C/T snv 0.11 10
rs3865188 0.790 0.320 16 82617112 intergenic variant A/G;T snv 10
rs4313119 0.776 0.080 8 127559610 intergenic variant G/T snv 0.27 10
rs4727012 0.790 0.080 7 149043401 intergenic variant C/T snv 0.12 10
rs4901473 0.776 0.080 14 53978439 regulatory region variant G/A snv 0.48 10
rs6469654 0.776 0.080 8 116620726 intergenic variant G/C snv 0.64 10
rs7160450 0.776 0.080 14 53990513 downstream gene variant T/C snv 0.48 10
rs76225372 0.790 0.080 10 19031157 intergenic variant A/G snv 7.4E-02 10
rs7708610 0.776 0.080 5 40102341 intergenic variant G/A;C snv 10
rs7794030 0.776 0.120 7 38712494 intergenic variant A/G snv 0.23 10
rs78341008 0.776 0.080 13 73217417 regulatory region variant T/C snv 4.8E-02 10
rs9271695 0.776 0.080 6 32625303 upstream gene variant A/G snv 0.76 10
rs9271770 0.776 0.120 6 32626471 upstream gene variant G/A snv 0.76 10
rs983402 0.776 0.080 2 198916862 intron variant T/C snv 0.62 10
rs9834244 0.776 0.120 3 151704793 intergenic variant G/A snv 6.1E-02 10
rs9930005 0.776 0.080 16 80009361 intergenic variant C/A;T snv 10
rs994308 0.776 0.080 20 6622975 intergenic variant C/T snv 0.43 10
rs10152518 0.790 0.080 15 67884824 intergenic variant G/A;T snv 9
rs1035209 0.790 0.080 10 99585609 intergenic variant C/T snv 0.15 9
rs10849438 0.790 0.080 12 6302870 intergenic variant T/G snv 1.0E-01 9
rs10951878 0.790 0.080 7 46887097 downstream gene variant C/A;T snv 9