| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S3688 | intron_variant | ZW10 | NM_004724.4:c.105+1291C>T | C/C | isolated CHD: ASD |
| S3689 | intron_variant | ZW10 | NM_004724.4:c.105+1291C>T | C/T | isolated CHD: ASD |
| S3690 | intron_variant | ZW10 | NM_004724.4:c.105+1291C>T | T/T | isolated CHD: ASD |
| S3691 | intron_variant | ZW10 | NM_004724.4:c.105+1291C>T | C | isolated CHD: ASD |
| S3692 | intron_variant | ZW10 | NM_004724.4:c.105+1291C>T | T | isolated CHD: ASD |