| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S4702 | missense_variant | RFC1 | NM_194255.4:c.80A>G | G/G | NA: NA |
| S4703 | missense_variant | RFC1 | NM_194255.4:c.80A>G | G/A | NA: NA |
| S4704 | missense_variant | RFC1 | NM_194255.4:c.80A>G | A/A | NA: NA |
| S4705 | missense_variant | RFC1 | NM_194255.4:c.80A>G | G/A+A/A | NA: NA |