Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs9282861 0.658 0.440 16 28606193 missense variant C/T snv 31
rs1042028 0.658 0.440 16 28606193 missense variant C/T snv 0.22 0.30 30
rs144848 0.653 0.440 13 32332592 missense variant A/C snv 0.28 0.23 29
rs3803662 0.662 0.440 16 52552429 non coding transcript exon variant A/G snv 0.63 25
rs2046210 0.708 0.280 6 151627231 intergenic variant G/A snv 0.41 21
rs2981582 0.695 0.360 10 121592803 intron variant A/G snv 0.58 21
rs13387042 0.732 0.280 2 217041109 intergenic variant A/G snv 0.44 16
rs72661131 0.742 0.480 10 52771739 upstream gene variant A/G snv 7.6E-04 15
rs34598529
HBB
0.724 0.280 11 5227100 5 prime UTR variant T/C snv 8.9E-04 14
rs10895068 0.752 0.240 11 101129483 5 prime UTR variant C/T snv 3.6E-02 14
rs562962093 0.742 0.520 10 52771740 upstream gene variant T/C snv 7.0E-06 13
rs549591993
F7
0.776 0.400 13 113105794 5 prime UTR variant C/A snv 4.0E-04 2.8E-05 12
rs10941679 0.763 0.120 5 44706396 intergenic variant A/G snv 0.25 11
rs63750953
HBB
0.790 0.400 11 5227097 5 prime UTR variant TT/- delins 7.0E-06 10
rs367732974
F7
0.790 0.360 13 113105788 5 prime UTR variant G/A snv 8.9E-05 2.8E-05 9
rs137852593
AR
0.827 0.160 X 67717484 missense variant G/A;C;T snv 2.2E-05; 1.1E-05; 9.1E-04 8
rs2981579 0.776 0.280 10 121577821 intron variant A/G snv 0.53 8
rs999737 0.776 0.200 14 68567965 intron variant C/T snv 0.16 8
rs6504950 0.807 0.120 17 54979110 intron variant G/A snv 0.29 7
rs137852573
AR
0.807 0.280 X 67686064 missense variant G/A snv 6
rs33931746
HBB
0.807 0.280 11 5227099 5 prime UTR variant T/C;G snv 6
rs34166473
HBD
0.827 0.320 11 5234513 5 prime UTR variant A/G snv 7.0E-06 6
rs35518301
HBD
0.827 0.200 11 5234514 5 prime UTR variant T/C snv 6