Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12951053 0.732 0.160 17 7674089 intron variant A/C snv 0.10 14
rs12947788 0.776 0.280 17 7674109 intron variant G/A snv 0.10 8
rs12602273 0.851 0.080 17 7679695 intron variant C/G snv 0.15 4
rs2078486 0.882 0.080 17 7679765 intron variant G/A;C snv 3
rs2287497 0.882 0.120 17 7689462 intron variant G/A snv 0.25 3
rs17880560 17 7668169 intron variant -/TGGCCG delins 2
rs59758982 0.925 0.040 17 7676326 intron variant TCCAGGTCCCCAGCCCTCCAGGTCCCCAGCCC/-;TCCAGGTCCCCAGCCC;TCCAGGTCCCCAGCCCTCCAGGTCCCCAGCCCTCCAGGTCCCCAGCCC delins 0.82 2
rs8078476 17 7677910 intron variant G/A snv 4.6E-02 2
rs8079544 1.000 0.040 17 7676734 intron variant C/T snv 7.4E-02 2
rs9894946 0.925 0.160 17 7667762 intron variant A/C;G snv 2
rs1555523630 1.000 0.120 17 7668202 intron variant -/C delins 1
rs1641549 17 7671457 intron variant C/T snv 0.35 1
rs35119871 17 7664197 intron variant C/T snv 0.22 1
rs397516436 0.641 0.440 17 7674894 stop gained G/A;C snv 34
rs786201059 0.701 0.360 17 7673764 stop gained C/A;G;T snv 20
rs876659384 0.851 0.240 17 7673552 stop gained C/A snv 7
rs201744589 0.882 0.240 17 7673728 stop gained C/A;G;T snv 4.0E-06; 1.2E-05 6
rs397516435 0.851 0.280 17 7674945 stop gained G/A;C snv 4.0E-06 6
rs121913344 0.925 0.200 17 7673704 stop gained G/A;T snv 5
rs121912652 0.882 0.200 17 7674191 stop gained C/A;T snv 4
rs730882029 0.882 0.200 17 7670685 stop gained G/A snv 4
rs879253911 0.925 0.200 17 7675074 stop gained C/A;T snv 4
rs1131691026 0.925 0.160 17 7675174 stop gained C/T snv 3
rs1429743956 0.882 0.080 17 7674906 stop gained T/A;C snv 3
rs730882001 0.925 0.200 17 7675119 stop gained G/A;T snv 3