Sensitive

Inborn genetic diseases

SCN1A · rs121918738

Stands on its own. Nothing else here links to this position yet — but the page above is the point: what the research found, what each genotype means, and where it came from, in language you can read. Links to conditions, drugs and the senses appear automatically if we write them.

Strength of the evidence

4 / 4

ClinVar classifies it as disease-causing (or likely), reviewed at 3 of 4 stars.

How this is scored

4: ClinVar disease-causing, reviewed by an expert panel or a guideline (3–4 stars). 3: ClinVar, several labs agreeing (2 stars), or a genetic study at p ≤ 10⁻⁵⁰. 2: ClinVar from one lab (1 star), or p ≤ 10⁻²⁰. 1: ClinVar submitted without criteria (0 stars), or genome-wide significance (p ≤ 5×10⁻⁸). The higher of the two counts. It says how solid the evidence is, not whether it matters for a particular person.

What ClinVar records

Classification Likely pathogenic for Inborn genetic diseases, Generalized epilepsy with febrile seizures plus, Early-infantile DEE; reviewed by expert panel (3 of 4 stars, 3 submitters), last evaluated 2024-04-30. ClinVar record 658067 NM_001165963.4(SCN1A):c.3629C>T (p.Thr1210Met)

Classification Pathogenic for Severe myoclonic epilepsy in infancy; criteria provided, single submitter (1 of 4 stars, 2 submitters), last evaluated 2014-12-20. ClinVar record 68617 NM_001165963.4(SCN1A):c.3629C>A (p.Thr1210Lys)

Change history MyGeneLog™ keeps a copy of every weekly release from 2026-10-19 and compares them. This position's classification has not changed since.

What this is ClinVar's aggregate record for this position (as of its 2026-11-01 release), not a result about you. A classification describes the variant against the condition named, as laboratories submitted it. Whether a person carries this variant, and what that would mean for them, is a question for a clinical test and a genetic counsellor.

How common each version is

AG

World gnomAD

G 100.0%

World TOPMed

G 100.0%

The share of all copies of this position that are each version. Source: the population studies published in dbSNP (US NCBI); each row names its study. No Korean figure for this position yet.

What each result means

A/A Two copies of the version ClinVar lists as likely disease-causing for Inborn genetic diseases. A result like this should be confirmed by a medical genetic test and talked through with a doctor; consumer DNA files can misread rare variants. (ClinVar VCV000658067, reviewed by expert panel)

A/G One copy of the version ClinVar lists as likely disease-causing for Inborn genetic diseases. Some conditions need only one copy; for others, one copy makes a person a carrier who is usually healthy but can pass it on. A genetic counsellor can say which applies. (ClinVar VCV000658067, reviewed by expert panel)

G/G No copy of the version ClinVar lists as likely disease-causing for Inborn genetic diseases. This is the usual result. (ClinVar VCV000658067, reviewed by expert panel)

Source: ClinVar VCV000658067, reviewed by expert panel

Quoting this page

Licensed CC BY-NC 4.0: free to read, share and adapt for non-commercial use, naming MyGeneLog™ and linking the exact page. Commercial use, including training or serving a commercial AI system, needs a licence — https://www.mygenelog.com/license

Inborn genetic diseases (rs121918738). MyGeneLog™. https://www.mygenelog.com/variants/rs121918738

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