| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S4686 | missense_variant | MTR | NM_000254.2:c.2756A>G | A/A | NA: NA |
| S4687 | missense_variant | MTR | NM_000254.2:c.2756A>G | A/G | NA: NA |
| S4688 | missense_variant | MTR | NM_000254.2:c.2756A>G | G/G | NA: NA |
| S4689 | missense_variant | MTR | NM_000254.2:c.2756A>G | A/G+G/G | NA: NA |
| S4727 | missense_variant | MTR | NM_000254.2:c.2756A>G | A/G | NA: NA |
| S4730 | missense_variant | MTR | NM_000254.2:c.2756A>G | A/G | NA: NA |