Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs7574865 0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs20417 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 57
rs1799969 0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02 38
rs1801198 0.677 0.400 22 30615623 missense variant G/A;C snv 5.6E-05; 0.57 26
rs12720356 0.752 0.360 19 10359299 missense variant A/C;G snv 6.1E-02; 4.0E-06 12
rs2294021 0.776 0.280 X 49249149 intron variant T/A;C snv 0.52 8
rs2812378 0.790 0.200 9 34710263 intron variant G/A;C snv 8
rs2246901 0.882 0.080 3 195762138 missense variant C/A;T snv 0.67 3