Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10020432
AFP
0.925 0.080 4 73455883 3 prime UTR variant A/G snv 0.54 2
rs10053538 0.807 0.160 5 157110499 intron variant C/A;T snv 7
rs1012068 0.827 0.160 22 31869917 intron variant T/G snv 0.37 5
rs10146249 1.000 0.080 14 92074996 intron variant C/A snv 0.29 1
rs10204525 0.701 0.440 2 241850169 3 prime UTR variant C/T snv 0.21 20
rs1041740 0.807 0.320 21 31667849 intron variant C/T snv 0.24 8
rs10433937 0.882 0.080 4 87308948 intron variant T/A;C;G snv 4
rs1049305 0.925 0.160 7 30924207 3 prime UTR variant G/C snv 0.52 4
rs1054690270 0.827 0.160 8 144505907 frameshift variant CT/- delins 5
rs1056836 0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs1059122 0.882 0.160 4 88726273 3 prime UTR variant T/A snv 0.46 3
rs10932029 0.827 0.200 2 203937045 intron variant T/A;C snv 5
rs10945859 0.882 0.120 6 162721570 intron variant T/C snv 0.17 3
rs11003123 0.827 0.200 10 52771774 upstream gene variant G/A snv 0.30 6
rs1127354 0.667 0.400 20 3213196 missense variant C/A;G snv 7.5E-02 26
rs1140409 0.925 0.080 17 64500552 missense variant A/C snv 5.4E-02 5.0E-02 2
rs11554495 0.701 0.240 12 52904798 missense variant C/A snv 4.9E-03 5.4E-03 19
rs1161457931 0.763 0.200 22 37084836 missense variant C/T snv 6.4E-06 9
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs11977021 0.827 0.240 7 106288069 upstream gene variant C/T snv 0.22 5
rs1201810520 0.925 0.160 2 88590497 missense variant C/T snv 2
rs12075 0.724 0.240 1 159205564 missense variant G/A snv 0.51 0.66 22
rs1208663703 0.763 0.200 22 37086414 missense variant T/C snv 5.2E-06 7.0E-06 9
rs12104272 0.925 0.080 19 49644795 intron variant G/A snv 0.44 2
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614