Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1188383936
F2
0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 102
rs777919630
CBS
0.623 0.680 21 43062358 missense variant G/A;T snv 8.0E-06; 4.0E-06 40
rs334
HBB
0.724 0.240 11 5227002 missense variant T/A;C;G snv 3.5E-03 35
rs35829419 0.689 0.560 1 247425556 missense variant C/A snv 3.9E-02 3.3E-02 23
rs887829 0.763 0.280 2 233759924 intron variant C/T snv 0.36 18
rs8175347 0.708 0.400 2 233760234 intron variant TATA/-;TA;TATATA;TATATATA;TATATATATA;TATATATATATA delins 16
rs9399137 0.851 0.320 6 135097880 intron variant T/C snv 0.20 13
rs11886868 0.752 0.280 2 60493111 intron variant C/T snv 0.65 12
rs1427407 0.827 0.120 2 60490908 intron variant T/C;G snv 6
rs3730070 0.925 0.120 12 48775065 intron variant G/C snv 0.13 0.23 2