Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 73
rs1056836 0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs13278062 0.807 0.200 8 23225458 non coding transcript exon variant G/A;C;T snv 8
rs153109 0.623 0.600 16 28507775 intron variant T/C snv 0.43 37
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs2070744 0.608 0.680 7 150992991 intron variant C/T snv 0.70 54
rs2073859 0.882 0.120 22 31278567 3 prime UTR variant G/A snv 4.0E-02 4
rs35592567 0.827 0.160 3 189896847 3 prime UTR variant C/G;T snv 6
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs401681 0.620 0.640 5 1321972 intron variant C/T snv 0.48 42
rs6983267 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 62
rs762551 0.701 0.400 15 74749576 intron variant C/A snv 0.67 23
rs798766 0.851 0.120 4 1732512 intron variant T/C snv 0.76 6
rs8034191 0.695 0.440 15 78513681 intron variant T/C snv 0.27 24
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs9282861 0.658 0.440 16 28606193 missense variant C/T snv 31
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs3218536 0.620 0.440 7 152648922 missense variant C/G;T snv 4.0E-06; 6.4E-02 37
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs17855750 0.695 0.480 16 28503907 missense variant A/C;T snv 6.4E-02; 4.0E-06 21
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs121434592 0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs78311289 0.689 0.440 4 1806162 missense variant A/C;G snv 4.0E-06 25