| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S2660 | intron_variant | GART | NM_032195.2:c.77+1138T>C | TT/TC/CC | NA: Normal echo |
| S2661 | intron_variant | GART | NM_032195.2:c.77+1138T>C | TC+TT/CC | NA: Normal echo |
| S2662 | intron_variant | GART | NM_032195.2:c.77+1138T>C | TT/TC+CC | NA: Normal echo |
| S2663 | intron_variant | GART | NM_032195.2:c.77+1138T>C | TC/TT+CC | NA: Normal echo |