| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S4690 | intron_variant | NFE2L2 | NC_000002.12:g.177253424C>T | C/C | NA: NA |
| S4691 | intron_variant | NFE2L2 | NC_000002.12:g.177253424C>T | C/T | NA: NA |
| S4692 | intron_variant | NFE2L2 | NC_000002.12:g.177253424C>T | T/T | NA: NA |
| S4693 | intron_variant | NFE2L2 | NC_000002.12:g.177253424C>T | C/T+T/T | NA: NA |