Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs867538330 0.925 0.080 5 102458457 synonymous variant C/T snv 2
rs230490 0.882 0.080 4 102466262 downstream gene variant G/A snv 0.34 3
rs35767 0.763 0.360 12 102481791 upstream gene variant A/C;G;T snv 13
rs28362491 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs28720239 1.000 0.080 4 102500998 non coding transcript exon variant ATTG/- delins 1
rs230510 1.000 0.080 4 102555009 intron variant T/A snv 0.37 1
rs3821958 1.000 0.080 4 102587667 intron variant A/G snv 0.42 1
rs3774959 0.925 0.080 4 102589957 intron variant G/A snv 0.34 2
rs3774964 1.000 0.080 4 102598330 intron variant A/G snv 0.39 1
rs997476 0.882 0.080 4 102620848 downstream gene variant G/T snv 4.3E-02 3
rs4450168 0.790 0.080 11 10265208 intron variant A/C;T snv 0.12 9
rs770635391 1.000 0.080 19 10271190 missense variant C/G;T snv 8.1E-06; 4.1E-06 1
rs750521832 0.732 0.200 11 102718452 missense variant A/G snv 4.0E-06 14
rs10883782 0.925 0.080 10 102824175 intron variant A/G snv 0.14 2
rs4919687 0.742 0.160 10 102835491 non coding transcript exon variant G/A snv 0.25 14
rs1799969 0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02 38
rs2094258 0.701 0.280 13 102844409 intron variant C/T snv 0.18 20
rs17724534 0.925 0.080 10 102845764 non coding transcript exon variant C/T snv 9.1E-02 2
rs751402 0.724 0.360 13 102845848 5 prime UTR variant A/G snv 0.76 15
rs2296147 0.695 0.280 13 102846025 5 prime UTR variant T/C snv 0.38 21
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs2276109 0.701 0.440 11 102875061 upstream gene variant T/C snv 9.2E-02 18
rs17655 0.597 0.560 13 102875652 missense variant G/C snv 0.28 0.30 52
rs873601 0.677 0.360 13 102875987 3 prime UTR variant G/A snv 0.59 25
rs26802 0.925 0.160 3 10290681 intron variant T/G snv 0.31 3