| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S4694 | missense_variant | MTRR | NM_024010.4:c.66A>G | A/A | NA: NA |
| S4695 | missense_variant | MTRR | NM_024010.4:c.66A>G | A/G | NA: NA |
| S4696 | missense_variant | MTRR | NM_024010.4:c.66A>G | G/G | NA: NA |
| S4697 | missense_variant | MTRR | NM_024010.4:c.66A>G | A/G+G/G | NA: NA |