SCN7A

sodium voltage-gated channel alpha subunit 7
OMIM: 182392, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Red SCN7A in Fetal anomalies


Level 2: Fetal (including NIPD)
Version 7.11
Latest signed off version: v7.0 (6 May 2026)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Literature
Phenotypes
  • Holoprosencephaly