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Familial infantile myoclonic epilepsy

TBC1D24 · rs545689324

Where this position leads

Condition: Epilepsy

rs545689324 Condition: Epilepsy Epilepsy Condition rs545689324 rs545689324 TBC1D24

Strength of the evidence

There is no record yet to score this position by (a ClinVar disease classification or a genome-wide significant study). That is not the same as weak evidence.

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 Conflicting classifications of pathogenicity for Familial infantile myoclonic epilepsy, Caused by mutation in the TBC1 domain family, member 24, Autosomal dominant nonsyndromic hearing loss 65, Developmental and epileptic encephalopathy, 1; criteria provided, conflicting classifications (1 of 4 stars, 3 submitters), last evaluated 2022-08-16. ClinVar record 436947 NM_001199107.2(TBC1D24):c.809G>A (p.Arg270His)

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 2026-10-19 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.

What each result means

A/A Two copies of the version labs disagree about for Familial infantile myoclonic epilepsy: in ClinVar, some labs call it disease-causing and others do not. 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 VCV000436947, criteria provided, conflicting classifications)
A/G One copy of the version labs disagree about for Familial infantile myoclonic epilepsy: in ClinVar, some labs call it disease-causing and others do not, so what one copy means is not settled. A genetic counsellor can look at the separate records. (ClinVar VCV000436947, criteria provided, conflicting classifications)
G/G No copy of the version labs disagree about for Familial infantile myoclonic epilepsy: in ClinVar, some labs call it disease-causing and others do not. This is the usual result. (ClinVar VCV000436947, criteria provided, conflicting classifications)

Source: ClinVar VCV000436947, criteria provided, conflicting classifications

Questions about rs545689324

What is rs545689324?

rs545689324 is a single position in the genome, in or near the TBC1D24 gene. Published research associates it with familial infantile myoclonic epilepsy. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs545689324 linked to?

On MyGeneLog this position is linked to Epilepsy. The research behind each link, and its sources, are set out on that condition page.

Does having rs545689324 mean I will get this?

No. Common variants like this one move a probability slightly and, on their own, rarely decide anything about one person. Nothing on this page is a diagnosis, and health decisions should be made with a clinician who can see your whole picture.

Where does the information about rs545689324 come from?

ClinVar VCV000436947, criteria provided, conflicting classifications. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

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

Familial infantile myoclonic epilepsy (rs545689324). MyGeneLog™. https://www.mygenelog.com/variants/rs545689324

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