Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs145204276 0.658 0.320 1 173868254 splice donor variant CAAGG/- delins 8.8E-02 31
rs351855 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 58
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 101
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs1444669684 0.658 0.480 9 21994285 missense variant C/A;T snv 36
rs1051740 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 56
rs2234922 0.630 0.440 1 225838705 missense variant A/G;T snv 0.19; 2.8E-05 42
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs2241880 0.627 0.600 2 233274722 missense variant A/G snv 0.45 0.44 37
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs2292832 0.605 0.640 2 240456086 non coding transcript exon variant T/A;C snv 0.59 46
rs1047840 0.708 0.280 1 241878999 missense variant G/A snv 0.36 0.40 19
rs121913240 0.672 0.440 12 25227342 missense variant T/A;C;G snv 24
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs1042028 0.658 0.440 16 28606193 missense variant C/T snv 0.22 0.30 30
rs9282861 0.658 0.440 16 28606193 missense variant C/T snv 31
rs6505162 0.695 0.320 17 30117165 5 prime UTR variant A/C;T snv 0.50; 3.1E-05 25
rs1202989817 0.716 0.360 21 31659813 missense variant T/C;G snv 8.0E-06 7.0E-06 18
rs1800624 0.658 0.480 6 32184610 upstream gene variant A/G;T snv 33
rs1800625 0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs876658657 0.677 0.280 3 37020356 missense variant A/G snv 4.0E-06 25
rs1056836 0.581 0.680 2 38071060 missense variant G/C snv 0.51 58