Variants
SCN1B variants
The SCN1B variant with a page here. Its page describes ClinVar's public record of the variant, never a result.
| Variant | Exon or intron | Position (GRCh38) | ClinVar classification | Review status |
|---|---|---|---|---|
| c.449-2A>G | Intron 3 | 35,039,115 | Pathogenic | 3 stars out of 4 reviewed by expert panel |