Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs964184 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 35
rs1047891 0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 25
rs334
HBB
0.724 0.240 11 5227002 missense variant T/A;C;G snv 3.5E-03 19
rs13331259 16 249924 intron variant A/G snv 3.0E-02 14
rs2853961 6 31264212 downstream gene variant G/A snv 0.38 13
rs112505971 10 27068541 intron variant A/C;G snv 13
rs3123543 1 212617344 intron variant T/A;C snv 13
rs3840870 17 50184820 3 prime UTR variant -/CTTG delins 13
rs76792961 16 243594 intron variant C/T snv 7.3E-03 13
rs9917425 20 16755400 intron variant G/T snv 0.16 13
rs7296503 12 41306962 intron variant C/T snv 0.57 13
rs4837892 9 121826025 intron variant G/T snv 0.36 13
rs35188965 5 1104823 intron variant C/G;T snv 12
rs3811444 1 247876149 missense variant C/T snv 0.31 0.26 12
rs7775698 1.000 0.080 6 135097497 intron variant C/T snv 6.9E-02 11
rs11065987 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 10
rs17758695 18 63253621 intron variant C/T snv 2.1E-02 10
rs603424 1.000 0.080 10 100315722 intron variant G/A snv 0.34 10
rs150813342 9 132989126 synonymous variant C/T snv 4.1E-03 4.1E-03 9
rs35979828 12 54292096 intron variant C/T snv 5.0E-02 9
rs11066301 0.827 0.200 12 112433568 intron variant A/G snv 0.30 7
rs6993770 0.925 0.080 8 105569300 intron variant A/T snv 0.31 7
rs385893 0.925 0.080 9 4763176 downstream gene variant T/C snv 0.44 6
rs11553699 12 121779004 3 prime UTR variant A/G snv 9.4E-02 6
rs11082304 18 23141009 intron variant G/C;T snv 5