Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs16139 0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02 36
rs8192678 0.667 0.440 4 23814039 missense variant C/T snv 0.31 0.26 28
rs237025 0.672 0.360 6 149400554 missense variant G/A snv 0.55 0.57 26
rs660339 0.695 0.320 11 73978059 missense variant G/A snv 0.41 0.43 24
rs14259 0.724 0.360 12 121915890 missense variant A/C;G snv 4.0E-06; 0.32 19
rs765798193 0.732 0.320 12 121915884 frameshift variant G/-;GG delins 18
rs713041 0.776 0.400 19 1106616 stop gained T/A;C snv 4.2E-06; 0.58 16
rs7756992 0.827 0.240 6 20679478 intron variant A/G;T snv 12
rs1549758 0.807 0.360 7 150998638 synonymous variant T/C snv 0.76 0.76 7
rs759853 0.827 0.320 7 134459206 non coding transcript exon variant G/A snv 0.33 6
rs1400094618
MOK
0.882 0.240 14 102229508 missense variant A/G snv 3
rs955333 0.882 0.240 6 154626274 intergenic variant A/G snv 0.13 3
rs6704078 0.925 0.200 1 216437370 intergenic variant C/T snv 0.94 2