| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S2692 | non_coding_transcript_exon_variant | MIR27A | NC_000019.10:g.13836478T>C | T/T | isolated CHD: VSD |
| S2693 | non_coding_transcript_exon_variant | MIR27A | NC_000019.10:g.13836478T>C | T/C | isolated CHD: VSD |
| S2694 | non_coding_transcript_exon_variant | MIR27A | NC_000019.10:g.13836478T>C | C/C | isolated CHD: VSD |
| S2695 | non_coding_transcript_exon_variant | MIR27A | NC_000019.10:g.13836478T>C | CC+CT/TT | isolated CHD: VSD |
| S2696 | non_coding_transcript_exon_variant | MIR27A | NC_000019.10:g.13836478T>C | CC/CT+TT | isolated CHD: VSD |