Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1154556 1.000 0.040 Y 21979249 intron variant T/C snv 1
rs6318 0.623 0.520 X 114731326 missense variant C/G;T snv 42
rs3027898 0.752 0.360 X 154010439 downstream gene variant C/A snv 11
rs3764880 0.752 0.320 X 12906707 start lost A/G snv 0.31 0.30 11
rs3764879 0.807 0.320 X 12906578 intron variant C/G snv 0.30 6
rs3761581 0.851 0.160 X 129655744 upstream gene variant A/C snv 0.11 5
rs763802417 0.882 0.040 X 100862805 missense variant G/A snv 5.9E-06 5
rs2968915 1.000 0.040 X 40580182 intron variant G/A snv 3
rs56204867 0.925 0.040 X 129656490 upstream gene variant A/G snv 0.11 3
rs755559514 0.925 0.040 X 129648648 missense variant T/C;G snv 1.2E-05; 6.1E-06 3
rs3115758 1.000 0.040 X 129647887 3 prime UTR variant C/A snv 0.21 0.31 1
rs3115759 1.000 0.040 X 129647539 3 prime UTR variant C/G;T snv 1
rs755622 0.611 0.720 22 23894205 intron variant G/C snv 0.26 44
rs1232898090 0.637 0.600 22 46198429 missense variant G/C;T snv 4.0E-06; 4.0E-06 40
rs4818 0.683 0.440 22 19963684 synonymous variant C/G;T snv 0.34 27
rs1801198 0.677 0.400 22 30615623 missense variant G/A;C snv 5.6E-05; 0.57 26
rs1065852 0.695 0.360 22 42130692 missense variant G/A snv 0.21 0.19 19
rs2071746 0.708 0.320 22 35380679 intron variant A/T snv 0.49 18
rs749437638 0.752 0.240 22 19968597 missense variant C/T snv 2.4E-05 1.4E-05 14
rs2096525 0.827 0.280 22 23894632 non coding transcript exon variant T/C snv 0.20 0.20 6
rs1007888 0.882 0.120 22 23898914 non coding transcript exon variant C/T snv 0.46 4
rs8141797 0.882 0.120 22 24186073 missense variant A/G snv 8.1E-02 9.8E-02 3
rs1081161 0.925 0.120 22 12200388 intergenic variant G/A snv 2
rs180803 0.925 0.080 22 24262890 intron variant G/A;T snv 2
rs6928 0.925 0.080 22 21760715 3 prime UTR variant C/G snv 0.49 2