Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1799971 0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs1801131 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs6313 0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs25531 0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs1800497 0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs2236225 0.614 0.640 14 64442127 missense variant G/A snv 0.44 0.38 52
rs1049353 0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs6311 0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 41
rs6277 0.689 0.480 11 113412737 synonymous variant G/A snv 0.41 0.38 36
rs1360780 0.708 0.320 6 35639794 intron variant T/A;C snv 31
rs4570625 0.724 0.200 12 71938143 upstream gene variant G/T snv 0.27 25
rs6296 0.732 0.160 6 77462543 synonymous variant C/G snv 0.31 0.27 23
rs1554210073 0.752 0.320 6 79042844 frameshift variant GT/A delins 21
rs2023239 0.724 0.160 6 88150763 intron variant T/C snv 0.21 20
rs5569 0.742 0.280 16 55697923 synonymous variant G/A;C snv 0.31; 4.0E-06 19
rs324981 0.724 0.320 7 34778501 missense variant A/T snv 0.44 0.47 18
rs1131691771 0.807 0.160 6 78958469 splice donor variant ACTT/- delins 18
rs1555565492 0.776 0.160 17 17795417 frameshift variant -/G delins 18
rs4290270 0.724 0.320 12 72022455 synonymous variant A/T snv 0.57 0.55 17
rs806368 0.752 0.280 6 88140381 3 prime UTR variant T/C snv 0.19 14
rs1562150844 0.790 0.280 6 78982908 frameshift variant CTTT/- delins 14