Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9296158 0.763 0.080 6 35599305 intron variant A/G snv 0.65 16
rs9470080 0.827 0.080 6 35678658 intron variant T/A;C snv 13
rs7997012 0.807 0.080 13 46837850 intron variant A/G snv 0.69 11
rs2242446 0.776 0.080 16 55656513 5 prime UTR variant C/A;T snv 9
rs11824092 0.925 0.080 11 13324747 intron variant T/C snv 0.62 7
rs120074175 0.827 0.080 12 72031544 missense variant G/A snv 1.2E-05 7.0E-06 7
rs139315125 0.851 0.080 1 7809900 missense variant A/G snv 5.6E-03 5.0E-03 7
rs2072621 0.851 0.080 X 151177387 non coding transcript exon variant C/A;G snv 7
rs2268498 0.827 0.080 3 8770725 intron variant T/C snv 0.41 7
rs2522833 0.827 0.080 7 82824392 missense variant A/C snv 0.45 0.34 7
rs57875989 0.882 0.080 1 7829913 splice acceptor variant GCTCTGTCCACAGGATCGCCTCCCATGAAGAATCCATCCCATCCTACTGCCAGC/-;GCTCTGTCCACAGGATCGCCTCCCATGAAGAATCCATCCCATCCTACTGCCAGCGCTCTGTCCACAGGATCGCCTCCCATGAAGAATCCATCCCATCCTACTGCCAGC delins 0.11 0.18 7
rs7766029 0.851 0.080 6 88137716 downstream gene variant T/C snv 0.51 7
rs10766075 0.925 0.080 11 13297040 intron variant C/T snv 0.27 6
rs1082214
MIP
0.925 0.080 12 56452706 non coding transcript exon variant C/T snv 9.3E-02 6
rs11022778 0.925 0.080 11 13369313 intron variant T/A;G snv 6
rs1409851868 0.882 0.080 3 89399325 missense variant A/G snv 6
rs1491850 0.925 0.080 11 27728178 intron variant T/C snv 0.37 6
rs156243 0.925 0.080 6 104416939 intergenic variant G/A snv 0.65 6
rs2253206 0.851 0.080 2 207527254 intron variant A/G snv 0.47 6
rs2291739 0.925 0.080 12 56420869 missense variant G/A;C snv 0.49; 4.0E-06 6
rs2619522 0.827 0.080 6 15653418 intron variant A/C snv 0.26 6
rs28386840 0.827 0.080 16 55652906 upstream gene variant T/A;C snv 6
rs3789327 0.925 0.080 11 13363769 intron variant A/G snv 0.53 6
rs1106634 0.851 0.080 8 20208538 intron variant G/A;C;T snv 0.18 5
rs11111 0.882 0.080 5 37814000 3 prime UTR variant T/C snv 0.22 5