SCN2A and Benign Familial Neonatal Epilepsy: Association Evidence

At a glance

Association overview

A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.

Provenance

1 source

Every contributing database and publication behind this association, with evidence type, strength, accessions and deep links.

SCN2A

2 source summaries

A gene summary alongside the source descriptions it was distilled from.

Benign Familial Neonatal Epilepsy

7 database identifiers

The disorder’s summary, prevalence, aliases and cross-reference identifiers (OMIM, Orphanet, MONDO, ICD-10, MedGen).

ClinVar and variant evidence

1,844 clinical variants

ClinVar variants reported for this pair, with disorder-specific significance, review status, molecular consequence and origin.

Literature

139 publications

Publications linking the gene and the disorder, with title, authors, journal, year and citation metrics.

Provenance

12 references

Every source and publication cited across this dossier, as one numbered reference list.