| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S1937 | missense_variant | RARS | NM_002887.4:c.7G>A | G/G | NA: Septa and valve abnormalities |
| S1938 | missense_variant | RARS | NM_002887.4:c.7G>A | A/G | NA: Septa and valve abnormalities |
| S1939 | missense_variant | RARS | NM_002887.4:c.7G>A | A/A | NA: Septa and valve abnormalities |