Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1047891 0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 25
rs79105258 12 111280427 intron variant C/A;T snv 23
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 21
rs334
HBB
0.724 0.240 11 5227002 missense variant T/A;C;G snv 3.5E-03 19
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 18
rs855791 0.701 0.400 22 37066896 missense variant A/G;T snv 0.57; 4.0E-06 17
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
rs7776054 6 135097778 intron variant A/G snv 0.24 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
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 12
rs3811444 1 247876149 missense variant C/T snv 0.31 0.26 12
rs198851 6 26104404 downstream gene variant T/A;C;G snv 11
rs7775698 1.000 0.080 6 135097497 intron variant C/T snv 6.9E-02 11
rs77542162 1.000 0.040 17 69085137 missense variant A/G snv 9.3E-03 1.0E-02 10
rs651821 0.851 0.360 11 116791863 5 prime UTR variant C/T snv 0.88 0.89 10
rs17758695 18 63253621 intron variant C/T snv 2.1E-02 10
rs2277339 12 56752285 missense variant T/G snv 0.12 0.14 10