Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1064797102 | 0.827 | 0.120 | 8 | 91071136 | splice acceptor variant | A/G | snv | 15 | |||
rs1562927768 | 0.790 | 0.080 | 7 | 105101476 | frameshift variant | AAAGA/- | delins | 15 | |||
rs759317757 | 0.807 | 0.280 | 8 | 91078416 | frameshift variant | TTAAC/- | delins | 12 | |||
rs1064797103 | 0.827 | 0.280 | 8 | 91078597 | missense variant | A/G | snv | 9 | |||
rs1554823375 | 0.851 | 0.160 | 10 | 1080454 | missense variant | C/T | snv | 8 | |||
rs368313959 | 0.851 | 0.080 | 8 | 91078383 | stop gained | C/T | snv | 1.6E-04 | 1.0E-04 | 8 | |
rs199722402 | 0.925 | 0.120 | 15 | 40987186 | missense variant | C/T | snv | 3.1E-04 | 8.4E-04 | 3 | |
rs372292910 | 1.000 | 0.040 | 5 | 141122905 | frameshift variant | A/-;AA | delins | 1.7E-04 | 3 | ||
rs730882226 | 0.925 | 0.120 | 15 | 41071953 | missense variant | A/G | snv | 1.6E-05 | 4.2E-05 | 3 | |
rs730882211 | 1.000 | 0.040 | 4 | 118815132 | missense variant | C/G | snv | 2 |