Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1131691014 | 0.439 | 0.800 | 17 | 7676154 | frameshift variant | -/C | ins | 214 | |||
rs3025058 | 0.658 | 0.600 | 11 | 102845217 | upstream gene variant | -/C;G | ins | 2.8E-04 | 26 | ||
rs28360317 | 0.716 | 0.280 | 5 | 83323739 | intron variant | -/CCT | delins | 0.24 | 15 | ||
rs1799732 | 0.790 | 0.160 | 11 | 113475529 | intron variant | -/G | delins | 11 | |||
rs1205454520 | 0.763 | 0.120 | 10 | 87864059 | 5 prime UTR variant | -/G | delins | 7.2E-06 | 10 | ||
rs11453459 | 0.882 | 0.080 | 19 | 52189696 | upstream gene variant | -/G | delins | 3 | |||
rs10680577 | 0.776 | 0.160 | 19 | 40798690 | intron variant | -/TACT | delins | 10 | |||
rs144848 | 0.653 | 0.440 | 13 | 32332592 | missense variant | A/C | snv | 0.28 | 0.23 | 29 | |
rs712 | 0.677 | 0.360 | 12 | 25209618 | 3 prime UTR variant | A/C | snv | 0.46 | 24 | ||
rs735482 | 0.742 | 0.160 | 19 | 45408744 | missense variant | A/C | snv | 0.21 | 0.20 | 16 | |
rs12951053 | 0.732 | 0.160 | 17 | 7674089 | intron variant | A/C | snv | 0.10 | 14 | ||
rs1057519697 | 0.776 | 0.120 | 2 | 29220830 | missense variant | A/C | snv | 12 | |||
rs1105879 | 0.790 | 0.240 | 2 | 233693556 | missense variant | A/C | snv | 0.35 | 0.34 | 11 | |
rs1204382931 | 0.790 | 0.160 | 2 | 38075270 | missense variant | A/C | snv | 4.3E-06 | 10 | ||
rs17486278 | 0.827 | 0.120 | 15 | 78575140 | intron variant | A/C | snv | 0.32 | 9 | ||
rs1057519729 | 0.827 | 0.080 | 15 | 66435113 | missense variant | A/C | snv | 6 | |||
rs11137037 | 0.851 | 0.200 | 8 | 6538661 | intron variant | A/C | snv | 0.40 | 4 | ||
rs2844337 | 0.851 | 0.120 | 11 | 77322663 | 3 prime UTR variant | A/C | snv | 0.28 | 4 | ||
rs425366 | 0.851 | 0.080 | 3 | 283727 | intron variant | A/C | snv | 0.56 | 4 | ||
rs9554314 | 0.851 | 0.080 | 13 | 28301652 | 3 prime UTR variant | A/C | snv | 4 | |||
rs1043973338 | 0.882 | 0.080 | 2 | 112830483 | missense variant | A/C | snv | 3 | |||
rs188912830 | 0.882 | 0.080 | X | 153981098 | non coding transcript exon variant | A/C | snv | 3 | |||
rs4713354 | 0.882 | 0.080 | 6 | 30717643 | upstream gene variant | A/C | snv | 0.22 | 3 | ||
rs7109645 | 0.882 | 0.080 | 11 | 77475278 | non coding transcript exon variant | A/C | snv | 0.29 | 3 | ||
rs7248167 | 0.882 | 0.080 | 19 | 43455962 | downstream gene variant | A/C | snv | 0.22 | 3 |