| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S0194 | missense_variant | MTHFD1 | NM_001364837.1:c.1958G>A | G/G | isolated CHD: other |
| S0195 | missense_variant | MTHFD1 | NM_001364837.1:c.1958G>A | G/A | isolated CHD: other |
| S0196 | missense_variant | MTHFD1 | NM_001364837.1:c.1958G>A | A/A | isolated CHD: other |
| S0197 | missense_variant | MTHFD1 | NM_001364837.1:c.1958G>A | G | isolated CHD: other |
| S0198 | missense_variant | MTHFD1 | NM_001364837.1:c.1958G>A | A | isolated CHD: other |