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 | 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 |