Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs889312 0.732 0.360 5 56736057 regulatory region variant C/A snv 0.69 14
rs36115365 0.807 0.160 5 1313127 upstream gene variant G/A;C;T snv 7
rs12413624 0.851 0.120 10 118519432 intergenic variant T/A snv 0.34 5
rs7675998 0.827 0.360 4 163086668 intergenic variant A/G;T snv 5
rs9502893 0.827 0.120 6 1339954 intergenic variant C/G;T snv 5
rs9564966 0.851 0.120 13 73322084 intergenic variant A/G snv 0.52 4
rs12029406 0.882 0.120 1 199936700 intergenic variant C/T snv 0.36 3
rs1517037 0.882 0.120 18 59211042 intergenic variant C/T snv 0.23 3
rs2980879 0.925 0.120 8 125469233 intron variant A/T snv 0.69 3
rs9363918 0.882 0.200 6 68432116 intron variant T/G snv 0.38 3
rs9543325 0.882 0.200 13 73342491 regulatory region variant C/G;T snv 3
rs10887710 0.925 0.120 10 80270029 downstream gene variant T/C snv 0.19 2
rs10919791 0.925 0.240 1 199996040 intergenic variant G/A snv 0.22 2
rs1552462 0.925 0.120 11 7235910 upstream gene variant C/T snv 2.7E-02 2
rs2816938 1.000 0.120 1 200016240 upstream gene variant T/A snv 0.37 2
rs6001516 0.925 0.120 22 39248198 intron variant C/T snv 6.1E-02 2
rs9573163 0.925 0.120 13 73334709 regulatory region variant C/G;T snv 2
rs12478462 1.000 0.120 2 152798206 intergenic variant T/G snv 0.28 1
rs1486134 1.000 0.120 2 67412637 downstream gene variant G/C;T snv 1
rs17275283 1.000 0.120 11 96970814 intron variant T/C snv 0.26 1
rs1944788 1.000 0.120 11 96947703 intron variant T/C snv 0.27 1
rs2218400 1.000 0.120 13 63564941 intergenic variant C/A snv 0.34 1
rs6537481 1.000 0.120 4 147474942 intergenic variant A/C;G snv 1
rs7330800 1.000 0.120 13 63573938 intergenic variant A/C;T snv 1
rs199976573
ABCG2
0.925 0.120 4 88132618 missense variant C/T snv 6.4E-05 5.6E-05 4