Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs771063992 | 0.827 | 0.240 | 5 | 34937431 | stop gained | C/T | snv | 2.8E-05 | 2.8E-05 | 7 | |
rs1555889984 | 0.925 | 0.120 | 21 | 34834536 | stop gained | C/A | snv | 5 | |||
rs121912651 | 0.605 | 0.680 | 17 | 7674221 | missense variant | G/A;C | snv | 4.0E-06 | 53 | ||
rs76992529 | 0.653 | 0.560 | 18 | 31598655 | missense variant | G/A | snv | 1.1E-03 | 4.9E-03 | 36 | |
rs1441937959 | 0.763 | 0.280 | 15 | 82240555 | missense variant | T/C | snv | 8.2E-06 | 20 | ||
rs28936375 | 0.752 | 0.320 | 1 | 53197092 | missense variant | C/A | snv | 1.7E-04 | 2.2E-04 | 15 | |
rs1114167422 | 0.776 | 0.320 | X | 154773148 | missense variant | A/G | snv | 11 | |||
rs121918544 | 0.827 | 0.200 | 14 | 24240635 | missense variant | C/T | snv | 7 | |||
rs768849283 | 0.882 | 0.040 | 10 | 70600517 | missense variant | C/G | snv | 6.8E-05 | 7 | ||
rs1057520529 | 0.851 | 0.320 | X | 49251440 | missense variant | C/T | snv | 5 | |||
rs28936072 | 0.851 | 0.200 | X | 154765472 | missense variant | T/C | snv | 4 | |||
rs774568856 | 0.882 | 0.200 | 6 | 83174481 | missense variant | A/G | snv | 1.7E-05 | 7.0E-06 | 4 | |
rs1057517674 | 0.925 | 0.040 | 1 | 11676926 | missense variant | A/T | snv | 2 | |||
rs878855337 | 0.925 | 0.120 | 7 | 93132385 | missense variant | C/G | snv | 2 | |||
rs1374309197 | 1.000 | 0.040 | 15 | 43492016 | missense variant | T/A;C | snv | 4.0E-06 | 7.0E-06 | 1 |