Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10887710 0.925 0.120 10 80270029 downstream gene variant T/C snv 0.19 2
rs12029406 0.882 0.120 1 199936700 intergenic variant C/T snv 0.36 3
rs12413624 0.851 0.120 10 118519432 intergenic variant T/A snv 0.34 5
rs1517037 0.882 0.120 18 59211042 intergenic variant C/T snv 0.23 3
rs1552462 0.925 0.120 11 7235910 upstream gene variant C/T snv 2.7E-02 2
rs2980879 0.925 0.120 8 125469233 intron variant A/T snv 0.69 3
rs36115365 0.807 0.160 5 1313127 upstream gene variant G/A;C;T snv 7
rs6001516 0.925 0.120 22 39248198 intron variant C/T snv 6.1E-02 2
rs7675998 0.827 0.360 4 163086668 intergenic variant A/G;T snv 5
rs889312 0.732 0.360 5 56736057 regulatory region variant C/A snv 0.69 14
rs9363918 0.882 0.200 6 68432116 intron variant T/G snv 0.38 3
rs9502893 0.827 0.120 6 1339954 intergenic variant C/G;T snv 5
rs9543325 0.882 0.200 13 73342491 regulatory region variant C/G;T snv 3
rs9564966 0.851 0.120 13 73322084 intergenic variant A/G snv 0.52 4
rs9573163 0.925 0.120 13 73334709 regulatory region variant C/G;T snv 2
rs199976573 0.925 0.120 4 88132618 missense variant C/T snv 6.4E-05 5.6E-05 4
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 34
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs150495372 0.925 0.120 4 99313834 missense variant C/T snv 3.7E-04 3
rs1693482 0.807 0.240 4 99342808 missense variant C/T snv 0.34 0.31 12
rs35385902 0.807 0.240 4 99347122 missense variant C/A;T snv 2.0E-05; 1.1E-03 9
rs698 0.724 0.240 4 99339632 missense variant T/A;C snv 0.35 20
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs4994 0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 65
rs1209809979 0.925 0.120 1 45568989 missense variant A/G snv 4.0E-06 3