Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2227631 | 0.742 | 0.200 | 7 | 101126257 | upstream gene variant | A/G | snv | 0.54 | 13 | ||
rs1799889 | 0.649 | 0.600 | 7 | 101126430 | upstream gene variant | A/G | snv | 31 | |||
rs3736234 | 0.851 | 0.040 | 12 | 10160535 | non coding transcript exon variant | G/A | snv | 0.40 | 4 | ||
rs5498 | 0.531 | 0.760 | 19 | 10285007 | missense variant | A/G | snv | 0.44 | 0.37 | 99 | |
rs974819 | 0.807 | 0.080 | 11 | 103789839 | intron variant | T/A;C | snv | 6 | |||
rs539179964 | 0.882 | 0.080 | 8 | 104248720 | missense variant | C/T | snv | 1.6E-05 | 4.2E-05 | 3 | |
rs4925 | 0.677 | 0.560 | 10 | 104263031 | missense variant | C/A | snv | 0.25 | 0.23 | 28 | |
rs28937313 | 0.882 | 0.160 | 9 | 104822520 | missense variant | T/C | snv | 8.0E-06 | 3 | ||
rs2066714 | 0.742 | 0.240 | 9 | 104824472 | missense variant | T/C | snv | 0.21 | 0.25 | 13 | |
rs4149313 | 0.763 | 0.240 | 9 | 104824472 | missense variant | T/C | snv | 9 | |||
rs2066715 | 0.807 | 0.160 | 9 | 104825752 | missense variant | C/T | snv | 8.2E-02 | 5.5E-02 | 7 | |
rs2230806 | 0.689 | 0.280 | 9 | 104858586 | missense variant | C/T | snv | 0.32 | 0.39 | 24 | |
rs17398575 | 0.882 | 0.040 | 7 | 106769006 | intron variant | G/A | snv | 0.20 | 3 | ||
rs6601530 | 1.000 | 0.040 | 8 | 10813762 | intron variant | G/A | snv | 0.61 | 1 | ||
rs3900940 | 0.827 | 0.040 | 3 | 108428881 | missense variant | T/A;C | snv | 4.3E-06; 0.24 | 6 | ||
rs2228315 | 0.807 | 0.120 | 12 | 108624122 | missense variant | C/T | snv | 0.11 | 0.14 | 7 | |
rs646776 | 0.752 | 0.240 | 1 | 109275908 | downstream gene variant | C/T | snv | 0.74 | 25 | ||
rs599839 | 0.724 | 0.360 | 1 | 109279544 | downstream gene variant | G/A;C | snv | 27 | |||
rs4773144 | 0.827 | 0.080 | 13 | 110308365 | intron variant | A/G | snv | 0.42 | 7 | ||
rs1122608 | 0.763 | 0.120 | 19 | 11052925 | intron variant | G/T | snv | 0.18 | 16 | ||
rs6511720 | 0.790 | 0.120 | 19 | 11091630 | intron variant | G/T | snv | 0.12 | 15 | ||
rs879254582 | 0.851 | 0.160 | 19 | 11105488 | frameshift variant | AGCCCCT/- | delins | 4 | |||
rs879254693 | 0.807 | 0.160 | 19 | 11107424 | missense variant | T/A;C;G | snv | 7 | |||
rs879254840 | 0.827 | 0.120 | 19 | 11113322 | missense variant | A/G | snv | 5 | |||
rs879254850 | 0.776 | 0.160 | 19 | 11113365 | missense variant | A/G;T | snv | 4.0E-06 | 9 |