| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S2664 | intron_variant | GART | NM_000819.5:c.1298+114G>C | GG/GC/CC | NA: Normal echo |
| S2665 | intron_variant | GART | NM_000819.5:c.1298+114G>C | GC+GG/CC | NA: Normal echo |
| S2666 | intron_variant | GART | NM_000819.5:c.1298+114G>C | GG/GC+CC | NA: Normal echo |
| S2667 | intron_variant | GART | NM_000819.5:c.1298+114G>C | GC/GG+CC | NA: Normal echo |