| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S2697 | non_coding_transcript_exon_variant | MIR499A | NC_000020.11:g.34990448A>G | A/A | isolated CHD: VSD |
| S2698 | non_coding_transcript_exon_variant | MIR499A | NC_000020.11:g.34990448A>G | G/A | isolated CHD: VSD |
| S2699 | non_coding_transcript_exon_variant | MIR499A | NC_000020.11:g.34990448A>G | G/G | isolated CHD: VSD |
| S2700 | non_coding_transcript_exon_variant | MIR499A | NC_000020.11:g.34990448A>G | GA+GG/AA | isolated CHD: VSD |
| S2701 | non_coding_transcript_exon_variant | MIR499A | NC_000020.11:g.34990448A>G | GG/GA+AA | isolated CHD: VSD |