| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S2677 | non_coding_transcript_exon_variant | MIR27A | NC_000019.10:g.13836478T>C | T/T | isolated CHD: ASD |
| S2678 | non_coding_transcript_exon_variant | MIR27A | NC_000019.10:g.13836478T>C | T/C | isolated CHD: ASD |
| S2679 | non_coding_transcript_exon_variant | MIR27A | NC_000019.10:g.13836478T>C | C/C | isolated CHD: ASD |
| S2680 | non_coding_transcript_exon_variant | MIR27A | NC_000019.10:g.13836478T>C | CC+CT/TT | isolated CHD: ASD |
| S2681 | non_coding_transcript_exon_variant | MIR27A | NC_000019.10:g.13836478T>C | CC/CT+TT | isolated CHD: ASD |