| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S3301 | missense_variant | MTHFD1 | NM_001364837.1:c.1958G>A | G | isolated CHD: PAD |
| S3302 | missense_variant | MTHFD1 | NM_001364837.1:c.1958G>A | G | isolated CHD: PAD |
| S3303 | missense_variant | MTHFD1 | NM_001364837.1:c.1958G>A | A | isolated CHD: PAD |
| S3304 | missense_variant | MTHFD1 | NM_001364837.1:c.1958G>A | A | isolated CHD: PAD |