Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
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
rs2234693 0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs25531 0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs9340799 0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs1143634 0.597 0.680 2 112832813 synonymous variant G/A snv 0.19 0.19 52
rs324420 0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26 48
rs1049353 0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
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
rs16139 0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02 36
rs746682028 0.645 0.480 11 27658414 missense variant C/A;T snv 4.0E-06; 4.0E-06 36
rs1006737 0.695 0.120 12 2236129 intron variant G/A snv 0.36 27
rs165599 0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56 27
rs4570625 0.724 0.200 12 71938143 upstream gene variant G/T snv 0.27 25
rs5522 0.732 0.320 4 148436323 missense variant C/T snv 0.88 0.89 19
rs4290270 0.724 0.320 12 72022455 synonymous variant A/T snv 0.57 0.55 17
rs9296158 0.763 0.080 6 35599305 intron variant A/G snv 0.65 16
rs3219151 0.752 0.160 5 161701908 3 prime UTR variant C/T snv 0.51 14
rs110402 0.790 0.120 17 45802681 intron variant G/A;C snv 12
rs4713916 0.790 0.160 6 35702206 intron variant A/C;G;T snv 11
rs7124442 0.827 0.160 11 27655494 3 prime UTR variant C/G;T snv 9