Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 35
rs79105258 12 111280427 intron variant C/A;T snv 23
rs334
HBB
0.724 0.240 11 5227002 missense variant T/A;C;G snv 3.5E-03 19
rs28601761 1.000 0.040 8 125487789 intron variant C/G snv 0.37 13
rs10821907 0.776 0.080 10 50888694 upstream gene variant C/T snv 0.20 12
rs12509595 1.000 0.080 4 80261400 intergenic variant T/C snv 0.23 10
rs10857147 1.000 0.040 4 80259918 intergenic variant A/T snv 0.25 9
rs10224210 1.000 0.040 7 151716108 intron variant T/C snv 0.21 8
rs62435145 1.000 0.040 7 1246931 regulatory region variant G/T snv 0.51 8
rs550057
ABO
0.925 0.080 9 133271182 intron variant T/A;C snv 7
rs760077 0.925 0.120 1 155208991 missense variant T/A snv 0.36 7
rs9895661 0.882 0.200 17 61379228 non coding transcript exon variant C/T snv 0.69 7
rs13146355 1.000 0.040 4 76490987 intron variant G/A snv 0.33 6
rs1533988 7 1253374 intergenic variant A/T snv 0.59 6
rs9472135 0.925 0.120 6 43842065 intron variant T/A;C;G snv 6
rs11072567 15 76006403 intron variant A/G snv 0.43 5
rs128494 21 36461960 intron variant T/C snv 0.72 4
rs2337106 18 48934533 intron variant C/A;G snv 4
rs6484504 11 31403276 intron variant T/C snv 0.79 3
rs7766720 6 106725104 non coding transcript exon variant T/C snv 0.16 3
rs11564722 11 2157100 intron variant C/T snv 0.25 2
rs4859682 4 76489165 intron variant C/A snv 0.33 2
rs6880621 5 34504277 intergenic variant G/A snv 0.55 2
rs7187776 16 28846324 5 prime UTR variant A/C;G snv 2
rs8080123 17 61165553 intron variant T/G snv 0.74 2