| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S2649 | intron_variant | GART | NM_032195.2:c.77+1138T>C | TC+TT/CC | isolated CHD: SD |
| S2650 | intron_variant | GART | NM_032195.2:c.77+1138T>C | TT/TC+CC | isolated CHD: SD |
| S2651 | intron_variant | GART | NM_032195.2:c.77+1138T>C | TC/TT+CC | isolated CHD: SD |
| S2652 | intron_variant | GART | NM_032195.2:c.77+1138T>C | TT/TC/CC | isolated CHD: SD |