Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs77375493 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 187
rs16906252 0.732 0.200 10 129467281 synonymous variant C/T snv 5.5E-02 5.1E-02 19
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 73
rs11547328 0.701 0.360 12 57751648 missense variant G/A;T snv 4.0E-06 27
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs2279744 0.605 0.640 12 68808800 intron variant T/G snv 0.31 48
rs746284240 0.763 0.240 12 68809243 missense variant A/G snv 11
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs767808984 0.851 0.160 14 36520098 missense variant C/G;T snv 1.3E-05 9
rs1048943 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
rs8034191 0.695 0.440 15 78513681 intron variant T/C snv 0.27 24
rs1800566 0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 59
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1057519747 0.716 0.280 17 7675094 missense variant A/C;G;T snv 23
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs11540652 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 57
rs121912651 0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 53
rs121912660 0.683 0.240 17 7673781 missense variant C/A;G;T snv 26
rs28934575 0.641 0.400 17 7674230 missense variant C/A;G;T snv 37
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 78
rs6505162 0.695 0.320 17 30117165 5 prime UTR variant A/C;T snv 0.50; 3.1E-05 25
rs730882025 0.724 0.360 17 7674885 missense variant C/A;G;T snv 21
rs762846821 0.614 0.320 17 7675151 missense variant C/A;T snv 8.0E-06 57
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs942158624 0.724 0.320 17 7674948 missense variant T/A snv 19