| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S3570 | intron_variant | FIGN | NC_000002.12:g.163641436C>G | G | NA: NA |
| S3571 | intron_variant | FIGN | NC_000002.12:g.163641436C>G | C | NA: NA |
| S3572 | intron_variant | FIGN | NC_000002.12:g.163641436C>G | G | NA: NA |
| S3573 | intron_variant | FIGN | NC_000002.12:g.163641436C>G | C | NA: NA |
| S3574 | intron_variant | FIGN | NC_000002.12:g.163641436C>G | G | NA: NA |
| S3575 | intron_variant | FIGN | NC_000002.12:g.163641436C>G | C | NA: NA |