Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs180177035 | 0.752 | 0.280 | 7 | 140801502 | missense variant | T/C | snv | 35 | |||
rs104894226 | 0.658 | 0.560 | 11 | 534285 | missense variant | C/A;G;T | snv | 23 | |||
rs121908120 | 0.701 | 0.280 | 2 | 218890289 | missense variant | T/A | snv | 1.4E-02 | 1.4E-02 | 7 | |
rs879253799 | 0.882 | 0.320 | 2 | 171443559 | frameshift variant | A/- | delins | 5 | |||
rs201249971 | 0.776 | 0.120 | 3 | 185519292 | missense variant | A/T | snv | 1.6E-04 | 4.9E-05 | 3 | |
rs587781245 | 0.882 | 0.120 | 6 | 148533885 | missense variant | G/A | snv | 6.8E-05 | 7.0E-05 | 3 | |
rs1057517491 | 0.776 | 0.240 | 13 | 20189448 | frameshift variant | C/- | delins | 2 | |||
rs72561723 | 0.790 | 0.240 | 13 | 20189448 | missense variant | C/T | snv | 8.0E-06 | 2 | ||
rs6457452 | 0.851 | 0.200 | 6 | 31827773 | 5 prime UTR variant | C/G;T | snv | 8.5E-05; 9.3E-02; 1.4E-05 | 1 | ||
rs12203592 | 0.649 | 0.320 | 6 | 396321 | intron variant | C/T | snv | 0.10 | 1 | ||
rs267607477 | 0.925 | 0.080 | 12 | 52567115 | missense variant | C/T | snv | 1 | |||
rs201868115 | 0.882 | 0.080 | 3 | 185519286 | missense variant | G/T | snv | 9.5E-05 | 2.8E-05 | 1 | |
rs199473704 | 0.882 | 0.080 | 17 | 3524224 | missense variant | C/A;T | snv | 1 | |||
rs121909800 | 0.807 | 0.360 | 12 | 47844859 | missense variant | G/A;T | snv | 1 |