| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S1698 | intron_variant | NOS3 | NM_000603.5:c.3106+11G>T | G/G | NA: NA |
| S1699 | intron_variant | NOS3 | NM_000603.5:c.3106+11G>T | G/T | NA: NA |
| S1700 | intron_variant | NOS3 | NM_000603.5:c.3106+11G>T | T/T | NA: NA |
| S1701 | intron_variant | NOS3 | NM_000603.5:c.3106+11G>T | G/G+G/T | NA: NA |