Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
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
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs1800566 0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 59
rs762846821 0.614 0.320 17 7675151 missense variant C/A;T snv 8.0E-06 57
rs17879961 0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 53
rs2279744 0.605 0.640 12 68808800 intron variant T/G snv 0.31 48
rs121913273 0.605 0.440 3 179218294 missense variant G/A;C snv 44
rs11571833 0.608 0.360 13 32398489 stop gained A/T snv 6.6E-03 6.0E-03 43
rs112445441 0.658 0.400 12 25245347 missense variant C/A;G;T snv 32
rs1800734 0.653 0.400 3 36993455 5 prime UTR variant G/A snv 0.22 30
rs876658657 0.677 0.280 3 37020356 missense variant A/G snv 4.0E-06 25
rs187115 0.695 0.320 11 35154612 intron variant T/C snv 0.37 22
rs12916300 0.742 0.080 15 28165345 intron variant C/T snv 0.50 13