| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs61750420 | 0.689 | 0.480 | 7 | 92501562 | missense variant | C/T | snv | 3.2E-04 | 3.5E-04 | 52 | |
| rs61750415 | 0.882 | 0.360 | 7 | 92503169 | frameshift variant | -/A | delins | 5.0E-04 | 5.1E-04 | 4 | |
| rs61750428 | 0.882 | 0.360 | 7 | 92494331 | stop gained | G/A;T | snv | 8.0E-06; 4.0E-06 | 4 | ||
| rs149806989 | 0.925 | 0.240 | 7 | 92517968 | stop gained | G/A | snv | 8.0E-06 | 3 | ||
| rs398123408 | 0.925 | 0.240 | 7 | 92504842 | protein altering variant | -/TCCACACTG | delins | 1.2E-05 | 2.1E-05 | 3 | |
| rs61750426 | 0.925 | 0.240 | 7 | 92494497 | frameshift variant | T/-;TTT | delins | 3.6E-05 | 5.6E-05 | 3 |