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Nemaline myopathy 2

NEB · rs1011425121

Where this position leads

Strength of the evidence

3 / 4

ClinVar classifies it as disease-causing (or likely), reviewed at 2 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 Nemaline myopathy 2, Arthrogryposis multiplex congenita 6, Nemaline myopathy; criteria provided, multiple submitters, no conflicts (2 of 4 stars, 4 submitters), last evaluated 2026-06-26. ClinVar record 557373 NM_001164508.2(NEB):c.23451+1G>C

Classification Conflicting classifications of pathogenicity for Nemaline myopathy 2, Arthrogryposis multiplex congenita 6; criteria provided, conflicting classifications (1 of 4 stars, 5 submitters), last evaluated 2026-05-21. ClinVar record 558659 NM_001164508.2(NEB):c.23451+1G>T

Classification Conflicting classifications of pathogenicity for Nemaline myopathy 2; criteria provided, conflicting classifications (1 of 4 stars, 2 submitters), last evaluated 2025-10-29. ClinVar record 2807215 NM_001164508.2(NEB):c.23451+1G>A

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

C/C No copy of the version ClinVar lists as likely disease-causing for Nemaline myopathy 2. This is the usual result. (ClinVar VCV000557373, criteria provided, multiple submitters, no conflicts)

C/G One copy of the version ClinVar lists as likely disease-causing for Nemaline myopathy 2. 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 VCV000557373, criteria provided, multiple submitters, no conflicts)

G/G Two copies of the version ClinVar lists as likely disease-causing for Nemaline myopathy 2. 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 VCV000557373, criteria provided, multiple submitters, no conflicts)

Source: ClinVar VCV000557373, criteria provided, multiple submitters, no conflicts

Questions about rs1011425121

What is rs1011425121?

rs1011425121 is a single position in the genome, in or near the NEB gene. Published research associates it with nemaline myopathy 2. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs1011425121 linked to?

On MyGeneLog this position is linked to Nemaline Myopathy 2. The research behind each link, and its sources, are set out on that condition page.

Does having rs1011425121 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 rs1011425121 come from?

ClinVar VCV000557373, criteria provided, multiple submitters, no conflicts. 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

Nemaline myopathy 2 (rs1011425121). MyGeneLog™. https://www.mygenelog.com/variants/rs1011425121

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