Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs71031566 1.000 0.080 10 94287212 non coding transcript exon variant -/ATTT ins 0.29 1
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs144848 0.653 0.440 13 32332592 missense variant A/C snv 0.28 0.23 29
rs712 0.677 0.360 12 25209618 3 prime UTR variant A/C snv 0.46 24
rs7763881 0.776 0.160 6 8653014 non coding transcript exon variant A/C snv 0.44 11
rs115797771 0.807 0.080 13 73064505 intron variant A/C snv 5.8E-02 6
rs2620381 1.000 0.080 15 42199650 mature miRNA variant A/C snv 4.4E-02 4.9E-02 1
rs2227981 0.763 0.400 2 241851121 synonymous variant A/C;G snv 1.6E-04; 0.63 12
rs213210 0.742 0.240 6 33208047 upstream gene variant A/C;G snv 11
rs1997623 0.807 0.160 7 116525306 missense variant A/C;G snv 0.86 9
rs1565684 1.000 0.080 8 18389154 upstream gene variant A/C;G snv 1
rs2032582 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs2273535 0.645 0.360 20 56386485 missense variant A/C;T snv 0.28 38
rs6505162 0.695 0.320 17 30117165 5 prime UTR variant A/C;T snv 0.50; 3.1E-05 25
rs762624 0.851 0.280 6 36677811 non coding transcript exon variant A/C;T snv 0.37; 2.4E-05 4
rs4359426 0.925 0.120 16 57358821 missense variant A/C;T snv 0.92 0.94 3
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs1799971 0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs1137101 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs17576 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 73