| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S4125 | missense_variant | HOXB1 | NM_002144.4:c.309A>T | A/A | isolated CHD: Pm VSD |
| S4126 | missense_variant | HOXB1 | NM_002144.4:c.309A>T | A/T | isolated CHD: Pm VSD |
| S4127 | missense_variant | HOXB1 | NM_002144.4:c.309A>T | T/T | isolated CHD: Pm VSD |