Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs34598529
HBB
0.724 0.280 11 5227100 5 prime UTR variant T/C snv 8.9E-04 14
rs33941377
HBB
0.752 0.080 11 5227158 5 prime UTR variant G/A;C;T snv 12
rs33944208
HBB
0.752 0.080 11 5227159 5 prime UTR variant G/A;C;T snv 12
rs11549407
HBB
0.752 0.080 11 5226774 stop gained G/A;C;T snv 3.3E-04 11
rs33915217
HBB
0.752 0.080 11 5226925 splice region variant C/A;G;T snv 4.0E-06; 5.9E-04; 4.0E-06 11
rs33986703
HBB
0.752 0.080 11 5226970 stop gained T/A;C;G snv 5.6E-05; 3.2E-05 11
rs35004220
HBB
0.752 0.080 11 5226820 non coding transcript exon variant C/T snv 1.6E-04 9.1E-05 11
rs33945777
HBB
0.763 0.080 11 5226576 splice donor variant C/A;G;T snv 4.0E-05 10
rs33971440
HBB
0.763 0.080 11 5226929 splice donor variant C/A;T snv 7.2E-05; 9.5E-05 10
rs34690599
HBB
0.763 0.080 11 5225832 intron variant G/C snv 2.8E-05 10
rs35724775
HBB
0.763 0.080 11 5226924 splice region variant A/G;T snv 1.2E-04 10
rs1141387
HBB
1.000 11 5226789 missense variant C/A;G snv 2
rs33929459
HBB
1.000 11 5226952 missense variant C/A;G;T snv 4.0E-06 2
rs33949869
HBB
1.000 11 5225606 missense variant A/C;G;T snv 2
rs33966487
HBB
0.925 0.040 11 5226588 missense variant C/G;T snv 2
rs33969677
HBB
0.925 0.080 11 5225714 missense variant C/A;G;T snv 2
rs33917628
HBB
1.000 11 5226623 missense variant C/G;T snv 1
rs33918338
HBB
1.000 11 5225611 missense variant T/A;C;G snv 4.0E-06 1
rs33921821
HBB
1.000 11 5225614 missense variant G/A;T snv 1
rs33937393
HBB
1.000 11 5226587 missense variant T/C;G snv 1
rs33951978
HBB
1.000 11 5226599 missense variant T/A;G snv 1
rs33954264
HBB
1.000 11 5225602 missense variant T/A;C;G snv 1
rs33954595
HBB
1.000 11 5226594 missense variant C/A;G;T snv 1
rs33959340
HBB
1.000 11 5226609 missense variant C/A;G;T snv 1
rs33961444
HBB
1.000 11 5225603 missense variant G/A;C snv 1