| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S3698 | intron_variant | ZW10 | NM_004724.4:c.1089+43T>A | T/T | isolated CHD: ASD/VSD/PDA/TOF/other |
| S3699 | intron_variant | ZW10 | NM_004724.4:c.1089+43T>A | T/A | isolated CHD: ASD/VSD/PDA/TOF/other |
| S3700 | intron_variant | ZW10 | NM_004724.4:c.1089+43T>A | A/A | isolated CHD: ASD/VSD/PDA/TOF/other |
| S3701 | intron_variant | ZW10 | NM_004724.4:c.1089+43T>A | T | isolated CHD: ASD/VSD/PDA/TOF/other |
| S3702 | intron_variant | ZW10 | NM_004724.4:c.1089+43T>A | A | isolated CHD: ASD/VSD/PDA/TOF/other |