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
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
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
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
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs25489 0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 78
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs12917 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 45
rs9344 0.653 0.480 11 69648142 splice region variant G/A snv 0.45 0.39 34
rs7799039 0.649 0.560 7 128238730 upstream gene variant G/A;C snv 33
rs187115 0.695 0.320 11 35154612 intron variant T/C snv 0.37 22
rs4696480 0.716 0.400 4 153685974 intron variant T/A snv 0.45 19
rs629849 0.827 0.160 6 160073377 missense variant A/C;G;T snv 0.90 0.91 9