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
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
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
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
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
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs4994 0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 65
rs6983267 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 62
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs2236225 0.614 0.640 14 64442127 missense variant G/A snv 0.44 0.38 52
rs1801157 0.611 0.600 10 44372809 3 prime UTR variant C/T snv 0.16 46