SCN2A Foundation · Global Registry

The SCN2A WorldMap

A privacy-first global registry of families affected by SCN2A-related disorders. Built to connect families, accelerate therapeutic research, and make our community visible to clinicians, regulators, and industry partners worldwide.

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Families on the Map

verified, approved

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Countries Represented

across six continents

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Unique Variants

LoF, GoF, Mixed, undetermined

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Global Distribution

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Loss of Function

Gain of Function

Mixed Function

Undetermined

City-level location only. Privacy by design.

Add Your Family

Join the WorldMap

Every pin is a family. Every family is a reason. Registration takes 90 seconds, and you control exactly what's visible.

Patient Information

First Name

Year of Birth

Sex at Birth

Variant Class

Specific Variant (optional) Helps connect you with families carrying the same variant globally.

Caregiver Contact

Email We'll send a confirmation and research updates based on your preferences below.

Location

Country *

City * City-level only. We never store precise coordinates.

What's Visible on the Map

Show my child's first name on the public pin Show year of birth Show variant class (LoF / GoF / Mixed)

Leave all unchecked to display only an anonymous pin.

How We May Contact You

Send me SCN2A Foundation updates: research news and family resources Allow other registered parents to contact me anonymously through the Foundation Notify me about clinical trials, natural history studies, and n=1 therapeutic programs relevant to my child's variant Allow vetted SCN2A advocacy organizations in my country to reach out

By submitting, you agree to our Privacy Policy and Terms of Use. Your location is stored at city level only, and you can edit or delete your record at any time.

01 / Privacy

Your data, your rules.

Location is stored at city level only. We geocode the city you provide to place your pin on the map. Display fields are off by default.

02 / Purpose

Why a map matters.

Visibility drives action. A registered, consented, geolocated cohort makes SCN2A unmissable to pharma, regulators, and funders, and it lets families with the same variant find each other across continents.

03 / Mission

Built for therapeutics.

The SCN2A Foundation is a research-driven 501(c)(3) focused exclusively on accelerating treatments for SCN2A-related disorders. Every registration directly supports our therapeutic development pipeline.