| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S2654 | intron_variant | GART | NM_000819.5:c.1298+114G>C | GG/GC/CC | isolated CHD: SD |
| S2656 | intron_variant | GART | NM_000819.5:c.1298+114G>C | GC+GG/CC | isolated CHD: SD |
| S2657 | intron_variant | GART | NM_000819.5:c.1298+114G>C | GG/GC+CC | isolated CHD: SD |
| S2658 | intron_variant | GART | NM_000819.5:c.1298+114G>C | GC/GG+CC | isolated CHD: SD |
| S2659 | intron_variant | GART | NM_000819.5:c.1298+114G>C | GG/GC/CC | isolated CHD: SD |