| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs104894010 | 1.000 | 0.080 | 7 | 44151048 | missense variant | A/G | snv | 1 | |||
| rs104894016 | 1.000 | 0.080 | 7 | 44145618 | missense variant | C/G;T | snv | 1 | |||
| rs1286804191 | 0.925 | 0.080 | 7 | 44145212 | missense variant | G/A | snv | 4.1E-06 | 1 | ||
| rs1554334579 | 1.000 | 0.080 | 7 | 44145577 | missense variant | G/T | snv | 1 | |||
| rs1554335612 | 1.000 | 0.080 | 7 | 44151068 | missense variant | T/A | snv | 1 | |||
| rs1554335616 | 1.000 | 0.080 | 7 | 44151075 | missense variant | G/C;T | snv | 1 | |||
| rs1554335752 | 1.000 | 0.080 | 7 | 44152339 | frameshift variant | A/- | del | 1 | |||
| rs1554335954 | 1.000 | 0.080 | 7 | 44153411 | missense variant | A/G;T | snv | 1 | |||
| rs193921338 | 1.000 | 0.080 | 7 | 44145590 | missense variant | G/A;T | snv | 4.4E-06; 4.4E-06 | 1 | ||
| rs193921340 | 1.000 | 0.080 | 7 | 44145581 | missense variant | A/G;T | snv | 1 | |||
| rs193922259 | 1.000 | 0.080 | 7 | 44153406 | stop gained | T/A | snv | 1 | |||
| rs193922261 | 1.000 | 0.080 | 7 | 44153402 | missense variant | C/G;T | snv | 4.0E-06 | 1 | ||
| rs193922262 | 0.925 | 0.080 | 7 | 44145636 | stop gained | C/A;G | snv | 4.3E-06 | 1 | ||
| rs193922263 | 1.000 | 0.080 | 7 | 44145626 | missense variant | G/A | snv | 1 | |||
| rs193922264 | 1.000 | 0.080 | 7 | 44145620 | missense variant | C/T | snv | 1 | |||
| rs193922265 | 1.000 | 0.080 | 7 | 44145614 | missense variant | G/C;T | snv | 1 | |||
| rs193922266 | 1.000 | 0.080 | 7 | 44145608 | missense variant | A/C;T | snv | 1 | |||
| rs193922267 | 1.000 | 0.080 | 7 | 44145597 | missense variant | C/T | snv | 1 | |||
| rs193922268 | 1.000 | 0.080 | 7 | 44145593 | missense variant | A/G | snv | 1 | |||
| rs193922269 | 1.000 | 0.080 | 7 | 44145575 | missense variant | C/A | snv | 1 | |||
| rs193922271 | 1.000 | 0.080 | 7 | 44145543 | missense variant | G/C;T | snv | 1 | |||
| rs193922272 | 1.000 | 0.080 | 7 | 44145510 | missense variant | T/C | snv | 1 | |||
| rs193922273 | 1.000 | 0.080 | 7 | 44145266 | missense variant | A/G;T | snv | 1 | |||
| rs193922274 | 1.000 | 0.080 | 7 | 44145176 | protein altering variant | GAGACCAGGGCCGCGCCCCGGCCACTGCCCTCCTCCGACTCGATGAAGGTGATCTCGCAGCTGGGCGTCAGCCTGCGCAC/TGTAA | delins | 1 | |||
| rs193922275 | 1.000 | 0.080 | 7 | 44145250 | frameshift variant | GC/- | delins | 1 |