Source: ALL
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
rs1799971 0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
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
rs53576 0.641 0.320 3 8762685 intron variant A/G;T snv 42
rs6311 0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 41
rs6295 0.645 0.200 5 63962738 intron variant C/G snv 0.49 40
rs1360780 0.708 0.320 6 35639794 intron variant T/A;C snv 31
rs165599 0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56 27
rs3800373 0.752 0.200 6 35574699 3 prime UTR variant C/A snv 0.68 22
rs4606 0.752 0.120 1 192812042 3 prime UTR variant C/G;T snv 16
rs1800532 0.763 0.160 11 18026269 intron variant G/T snv 0.33 15
rs3219151 0.752 0.160 5 161701908 3 prime UTR variant C/T snv 0.51 14
rs1042173 0.763 0.320 17 30197993 3 prime UTR variant A/C snv 0.40 14
rs734312 0.790 0.240 4 6301627 missense variant G/A snv 0.55 0.42 10
rs636832 0.790 0.400 1 35897874 intron variant G/A snv 0.23 8
rs3796863 0.790 0.160 4 15848363 intron variant G/T snv 0.41 8
rs11568817 0.790 0.120 6 77463665 5 prime UTR variant A/C snv 0.37 8
rs130058 0.790 0.120 6 77463564 5 prime UTR variant T/A;G snv 8
rs3813034 0.827 0.160 17 30197786 3 prime UTR variant A/C snv 0.40 8
rs9332377 0.882 0.120 22 19968169 intron variant C/A;T snv 5
rs3757 0.851 0.160 22 20111808 3 prime UTR variant G/A snv 0.21 5
rs1867283 0.925 0.080 9 84835851 intron variant G/A snv 0.39 5