| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S1546 | intron_variant | CUBN | NC_000010.11:g.17088694A>G | A/G+G/G | NA: NA |
| S1547 | intron_variant | CUBN | NC_000010.11:g.17088694A>G | g.17088694A>G | NA: NA |
| S1548 | intron_variant | CUBN | NC_000010.11:g.17088694A>G | g.17088694A>G | NA: NA |