| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S3254 | non_coding_transcript_exon_variant | MIR196A2 | NR_029617.1:n.78C>T | C | NA: NA |
| S3255 | non_coding_transcript_exon_variant | MIR196A2 | NR_029617.1:n.78C>T | T | NA: NA |
| S3256 | non_coding_transcript_exon_variant | MIR196A2 | NR_029617.1:n.78C>T | C | NA: NA |
| S3257 | non_coding_transcript_exon_variant | MIR196A2 | NR_029617.1:n.78C>T | T | NA: NA |