Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs735482 0.742 0.160 19 45408744 missense variant A/C snv 0.21 0.20 16
rs1057520001 0.677 0.360 17 7674886 missense variant A/C;G snv 23
rs17879961 0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 53
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs1137101 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
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
rs1800625 0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs2274223 0.620 0.400 10 94306584 missense variant A/G snv 0.28 0.31 40
rs3087386 0.790 0.160 2 99439044 missense variant A/G snv 0.58 0.61 8
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs751402 0.724 0.360 13 102845848 5 prime UTR variant A/G snv 0.76 15
rs876658657 0.677 0.280 3 37020356 missense variant A/G snv 4.0E-06 25
rs937283 0.716 0.200 12 68808384 5 prime UTR variant A/G snv 0.37 19
rs11571833 0.608 0.360 13 32398489 stop gained A/T snv 6.6E-03 6.0E-03 43
rs4073 0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 64
rs1899663 0.683 0.280 12 53967210 intron variant C/A snv 0.28 22
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs121913530 0.583 0.640 12 25245351 missense variant C/A;G;T snv 63
rs1799793 0.557 0.640 19 45364001 missense variant C/A;T snv 7.1E-06; 0.29 72
rs1801270 0.689 0.400 6 36684194 missense variant C/A;T snv 0.15; 4.4E-05 22
rs762846821 0.614 0.320 17 7675151 missense variant C/A;T snv 8.0E-06 57
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147