Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
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
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 9
rs2979489 8 30423317 intron variant G/A;C snv 6
rs3809627 16 30091839 5 prime UTR variant C/A snv 0.41 5
rs62160676 2 111410354 intron variant T/C;G snv 5
rs78744187 19 33263642 intergenic variant C/T snv 6.8E-02 5