| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S3293 | missense_variant | MTHFD1 | NM_001364837.1:c.1958G>A | G | isolated CHD: ASD |
| S3294 | missense_variant | MTHFD1 | NM_001364837.1:c.1958G>A | G | isolated CHD: ASD |
| S3295 | missense_variant | MTHFD1 | NM_001364837.1:c.1958G>A | A | isolated CHD: ASD |
| S3296 | missense_variant | MTHFD1 | NM_001364837.1:c.1958G>A | A | isolated CHD: ASD |