Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs41274221 0.851 0.160 7 100093577 mature miRNA variant C/T snv 6.4E-05 4.9E-05 6
rs4919510 0.641 0.520 10 100975021 mature miRNA variant C/G snv 0.27 0.27 32
rs61991156 0.925 0.080 14 101022077 mature miRNA variant A/G snv 2
rs16999593 0.742 0.240 19 10180505 missense variant T/C snv 2.4E-02 9.6E-03 14
rs3732131 0.925 0.080 2 102178143 3 prime UTR variant A/G snv 0.12 2
rs3771157 0.925 0.080 2 102396972 3 prime UTR variant C/A snv 3.7E-02 2
rs1135354 0.925 0.080 2 102397842 3 prime UTR variant T/G snv 0.23 3
rs6218 0.732 0.440 12 102399855 3 prime UTR variant A/G snv 2.1E-02 13
rs1520220 0.807 0.280 12 102402744 intron variant G/C;T snv 0.76 9
rs4764887 0.925 0.080 12 102430122 intron variant G/A snv 2.2E-02 2
rs1536309 0.851 0.160 10 102435445 upstream gene variant A/G snv 0.32 7
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 20
rs5742612 0.752 0.440 12 102481086 intron variant A/G snv 5.6E-02 11
rs28362491 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs4648068 0.790 0.240 4 102597148 intron variant A/G snv 0.31 9
rs3774968 0.882 0.120 4 102609955 intron variant A/G snv 0.64 4
rs1799750 0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs2094258 0.701 0.280 13 102844409 intron variant C/T snv 0.18 20
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
rs1047768 0.695 0.320 13 102852167 synonymous variant T/C snv 0.52 0.59 20
rs2227869 0.790 0.240 13 102862735 missense variant G/A;C snv 4.3E-02 9
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