| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S3770 | non_coding_transcript_exon_variant | MIR138-2 | NC_000016.10:g.56858519G>T | G/G | isolated CHD: TOF |
| S3771 | non_coding_transcript_exon_variant | MIR138-2 | NC_000016.10:g.56858519G>T | G/T | isolated CHD: TOF |
| S3772 | non_coding_transcript_exon_variant | MIR138-2 | NC_000016.10:g.56858519G>T | G | isolated CHD: TOF |
| S3773 | non_coding_transcript_exon_variant | MIR138-2 | NC_000016.10:g.56858519G>T | T | isolated CHD: TOF |