| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S0419 | non_coding_transcript_exon_variant | MIR499A | NR_030223.1:n.73A>G | A/A | NA: NA |
| S0420 | non_coding_transcript_exon_variant | MIR499A | NR_030223.1:n.73A>G | A/G | NA: NA |
| S0421 | non_coding_transcript_exon_variant | MIR499A | NR_030223.1:n.73A>G | G/G | NA: NA |
| S0425 | non_coding_transcript_exon_variant | MIR499A | NR_030223.1:n.73A>G | A/A | NA: NA |
| S0426 | non_coding_transcript_exon_variant | MIR499A | NR_030223.1:n.73A>G | A/G | NA: NA |
| S0427 | non_coding_transcript_exon_variant | MIR499A | NR_030223.1:n.73A>G | G/G | NA: NA |