| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S0485 | intron_variant | ISL1 | NM_002202.3:c.28+17C>T | C/C | NA: NA, AVR |
| S0486 | intron_variant | ISL1 | NM_002202.3:c.28+17C>T | C/T | NA: NA, AVR |
| S0493 | intron_variant | ISL1 | NM_002202.3:c.28+17C>T | C/C | NA: NA, AVR |
| S0494 | intron_variant | ISL1 | NM_002202.3:c.28+17C>T | C/T | NA: NA, AVR |