| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S3767 | non_coding_transcript_exon_variant | MIR138-2 | NC_000016.10:g.56858681G>A | A/A | isolated CHD: VSD/ASD/TOF/PDA |
| S3768 | non_coding_transcript_exon_variant | MIR138-2 | NC_000016.10:g.56858681G>A | G | isolated CHD: VSD/ASD/TOF/PDA |
| S3769 | non_coding_transcript_exon_variant | MIR138-2 | NC_000016.10:g.56858681G>A | A | isolated CHD: VSD/ASD/TOF/PDA |