Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs334
HBB
0.724 0.240 11 5227002 missense variant T/A;C;G snv 3.5E-03 35
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 28
rs2814778 0.763 0.360 1 159204893 5 prime UTR variant T/C snv 0.25 24
rs635634 0.882 0.160 9 133279427 upstream gene variant T/A;C snv 22
rs1800961 0.851 0.160 20 44413724 missense variant C/T snv 3.1E-02 2.5E-02 21
rs2519093
ABO
0.882 0.200 9 133266456 intron variant T/C snv 16
rs7705526 0.776 0.240 5 1285859 intron variant C/A;T snv 15
rs13331259 16 249924 intron variant A/G snv 3.0E-02 14
rs112505971 10 27068541 intron variant A/C;G snv 13
rs2853961 6 31264212 downstream gene variant G/A snv 0.38 13
rs3123543 1 212617344 intron variant T/A;C snv 13
rs3840870 17 50184820 3 prime UTR variant -/CTTG delins 13
rs4837892 9 121826025 intron variant G/T snv 0.36 13
rs7296503 12 41306962 intron variant C/T snv 0.57 13
rs76792961 16 243594 intron variant C/T snv 7.3E-03 13
rs9917425 20 16755400 intron variant G/T snv 0.16 13
rs174549 0.851 0.240 11 61803910 5 prime UTR variant G/A snv 0.26 12
rs35188965 5 1104823 intron variant C/G;T snv 12
rs17758695 18 63253621 intron variant C/T snv 2.1E-02 10
rs218265 4 54542832 intergenic variant T/C snv 0.21 10
rs12239046 1 247438293 intron variant T/C snv 0.58 9
rs150813342 9 132989126 synonymous variant C/T snv 4.1E-03 4.1E-03 9