Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs483143 0.925 0.080 6 27878966 intergenic variant G/C snv 0.13 2
rs62081501 0.925 0.080 18 37627749 intron variant G/A snv 6.2E-02 4
rs7867155 0.925 0.080 9 96065532 intron variant C/T snv 0.13 2
rs8067056 0.925 0.080 17 46006582 intron variant T/C;G snv 0.30 5
rs9296158 0.763 0.080 6 35599305 intron variant A/G snv 0.65 16
rs9980603 0.925 0.080 21 40514656 intron variant T/C snv 0.40 2
rs1006737 0.695 0.120 12 2236129 intron variant G/A snv 0.36 27
rs110402 0.790 0.120 17 45802681 intron variant G/A;C snv 12
rs12938031 0.851 0.160 17 45777136 intron variant A/G snv 0.26 6
rs3219151 0.752 0.160 5 161701908 3 prime UTR variant C/T snv 0.51 14
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
rs1390938 0.807 0.200 8 20179202 missense variant A/G snv 0.71 0.78 7
rs4570625 0.724 0.200 12 71938143 upstream gene variant G/T snv 0.27 25
rs6295 0.645 0.200 5 63962738 intron variant C/G snv 0.49 40
rs7209436 0.851 0.200 17 45792776 intron variant C/T snv 0.43 5
rs165599 0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56 27
rs4290270 0.724 0.320 12 72022455 synonymous variant A/T snv 0.57 0.55 17
rs53576 0.641 0.320 3 8762685 intron variant A/G;T snv 42
rs5522 0.732 0.320 4 148436323 missense variant C/T snv 0.88 0.89 19
rs324420 0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26 48
rs746682028 0.645 0.480 11 27658414 missense variant C/A;T snv 4.0E-06; 4.0E-06 36
rs25531 0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs16139 0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02 36
rs1049353 0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42