Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs775104326 0.776 0.160 3 41224995 stop gained C/A;T snv 4.0E-06 10
rs587782177 0.763 0.200 17 7674887 missense variant C/A;G;T snv 11
rs121913403 0.683 0.240 3 41224622 missense variant C/A;G;T snv 23
rs28931589 0.695 0.240 3 41224613 missense variant G/A;C;T snv 17
rs967461896 0.724 0.240 17 7675086 missense variant A/C;G;T snv 17
rs1057519747 0.716 0.280 17 7675094 missense variant A/C;G;T snv 23
rs1064793929 0.882 0.280 17 7675167 frameshift variant A/-;AA delins 5
rs2107425 0.732 0.280 11 1999845 intron variant C/T snv 16
rs753660142 0.708 0.280 17 7673782 missense variant T/C;G snv 1.6E-05 19
rs985033810 0.724 0.280 17 7674232 missense variant C/A;G;T snv 16
rs1057519997 0.776 0.320 17 7676037 missense variant A/C;G;T snv 9
rs121913274 0.645 0.320 3 179218304 missense variant A/C;G;T snv 33
rs2066827 0.695 0.320 12 12718165 missense variant T/A;C;G snv 1.6E-04; 1.6E-05; 0.26 21
rs2516839 0.732 0.320 1 161043331 5 prime UTR variant C/T snv 0.49 14
rs587780070 0.683 0.320 17 7675077 missense variant G/A;C;T snv 4.0E-06 24
rs752742313 0.637 0.320 3 138655502 missense variant C/T snv 1.2E-05 36
rs864622237 0.716 0.320 17 7674263 missense variant A/C;G;T snv 17
rs121912666 0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 34
rs121913400 0.683 0.360 3 41224610 missense variant C/A;G;T snv 26
rs148924904 0.724 0.360 17 7675124 missense variant T/C snv 7.0E-06 17
rs17251221 0.724 0.360 3 122274400 intron variant A/G snv 0.11 18
rs2273535 0.645 0.360 20 56386485 missense variant A/C;T snv 0.28 38
rs28934571 0.645 0.360 17 7674216 missense variant C/A;G snv 31
rs786201059 0.701 0.360 17 7673764 stop gained C/A;G;T snv 20
rs876660754 0.701 0.360 17 7675095 missense variant C/A;T snv 20