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
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
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
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs6983267 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 62
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
rs397517132 0.623 0.280 7 55191846 missense variant A/T snv 48
rs1205
CRP
0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 46
rs1801157 0.611 0.600 10 44372809 3 prime UTR variant C/T snv 0.16 46
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 38
rs112445441 0.658 0.400 12 25245347 missense variant C/A;G;T snv 32
rs760043106 0.645 0.440 17 7674947 missense variant A/C;G;T snv 32
rs121913227 0.653 0.320 7 140753336 missense variant AC/CT;TT mnv 31
rs1800734 0.653 0.400 3 36993455 5 prime UTR variant G/A snv 0.22 30
rs752021744 0.689 0.440 3 138759306 missense variant T/C snv 1.2E-05 29
rs712 0.677 0.360 12 25209618 3 prime UTR variant A/C snv 0.46 24