Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3512 0.925 0.160 15 30942802 3 prime UTR variant G/C snv 0.27 4
rs104894393 0.925 0.120 13 101726785 missense variant A/G snv 2
rs3864180 1.000 0.040 13 91784234 intron variant A/G;T snv 1
rs334
HBB
0.724 0.240 11 5227002 missense variant T/A;C;G snv 3.5E-03 35
rs9399137 0.851 0.320 6 135097880 intron variant T/C snv 0.20 13
rs1805015 0.683 0.520 16 27362859 missense variant T/C snv 0.16 0.22 22
rs1805123 0.724 0.280 7 150948446 missense variant T/A;C;G snv 1.3E-05; 0.18; 8.4E-06 18
rs767910122 0.724 0.280 7 150948446 frameshift variant -/GTCCG ins 4.4E-05 17
rs794728448 0.724 0.280 7 150948445 frameshift variant CT/G delins 17
rs120074192 0.763 0.120 11 2527959 missense variant A/G snv 10
rs12720459 0.807 0.160 11 2583535 missense variant C/A;G;T snv 7
rs116928232 0.827 0.120 10 89222511 missense variant C/G;T snv 1.2E-05; 9.1E-04 9
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs35829419 0.689 0.560 1 247425556 missense variant C/A snv 3.9E-02 3.3E-02 23
rs111033560 0.807 0.040 6 118559037 stop gained T/G snv 1.6E-05 9
rs1805323 0.925 0.160 7 5987311 missense variant G/A;T snv 4.0E-06; 8.0E-02 2
rs113994095 0.701 0.360 15 89327201 missense variant C/T snv 5.1E-04 6.7E-04 31
rs1458500258 0.925 0.080 1 237388098 missense variant G/T snv 7.0E-06 3
rs11720524 0.882 0.080 3 38633921 intron variant C/G;T snv 0.34 3
rs138694505 1.000 0.040 7 84007493 missense variant T/C snv 3.4E-03 6.6E-03 1
rs4149000 0.882 0.080 12 21295063 non coding transcript exon variant C/T snv 0.11 5
rs11567847 0.925 0.120 11 12937202 missense variant T/C snv 3
rs606231451 0.925 0.120 1 1535372 missense variant G/A snv 2
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