Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs112445441 0.658 0.400 12 25245347 missense variant C/A;G;T snv 32
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs1179251 0.763 0.320 12 68251271 intron variant C/G snv 0.18 14
rs1205
CRP
0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 46
rs121913227 0.653 0.320 7 140753336 missense variant AC/CT;TT mnv 31
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs1284806277
MOK
0.827 0.200 14 102251978 missense variant A/G snv 1.4E-05 13
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs1800734 0.653 0.400 3 36993455 5 prime UTR variant G/A snv 0.22 30
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
rs2555639 0.851 0.080 4 174540379 non coding transcript exon variant T/C snv 0.38 7
rs28929495 0.807 0.120 7 55174014 missense variant G/A;C;T snv 9
rs35301225 0.882 0.080 1 9151743 mature miRNA variant C/A;T snv 5
rs3775292 0.851 0.080 4 186081871 non coding transcript exon variant C/G snv 0.82 5
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs397517132 0.623 0.280 7 55191846 missense variant A/T snv 48
rs60745952 0.925 0.080 4 148827842 intron variant T/C snv 0.13 6
rs6983267 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 62
rs712 0.677 0.360 12 25209618 3 prime UTR variant A/C snv 0.46 24
rs760043106 0.645 0.440 17 7674947 missense variant A/C;G;T snv 32
rs77191406 0.790 0.280 6 137881704 3 prime UTR variant C/T snv 7.2E-04 12
rs7758229 0.732 0.120 6 160419220 intron variant G/A;T snv 16
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs992157 0.790 0.080 2 218290058 5 prime UTR variant G/A snv 0.46 10