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Neurofibromatosis, type 1

NF1 · rs1567848711

Where this position leads

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 Likely benign for Neurofibromatosis, type 1; criteria provided, multiple submitters, no conflicts (2 of 4 stars, 3 submitters), last evaluated 2026-01-04. ClinVar record 561783 NM_001042492.3(NF1):c.2410-13A>T

Classification Pathogenic/Likely pathogenic for Neurofibromatosis, type 1, NF1-related disorder; criteria provided, multiple submitters, no conflicts (2 of 4 stars, 6 submitters), last evaluated 2025-04-01. ClinVar record 804167 NM_001042492.3(NF1):c.2410-13A>G

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 No copy of the version ClinVar lists as disease-causing or likely disease-causing for Neurofibromatosis, type 1. This is the usual result. (ClinVar VCV000804167, criteria provided, multiple submitters, no conflicts)

A/G One copy of the version ClinVar lists as disease-causing or likely disease-causing for Neurofibromatosis, type 1. 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 VCV000804167, criteria provided, multiple submitters, no conflicts)

G/G Two copies of the version ClinVar lists as disease-causing or likely disease-causing for Neurofibromatosis, type 1. 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 VCV000804167, criteria provided, multiple submitters, no conflicts)

Source: ClinVar VCV000804167, criteria provided, multiple submitters, no conflicts

Questions about rs1567848711

What is rs1567848711?

rs1567848711 is a single position in the genome, in or near the NF1 gene. Published research associates it with neurofibromatosis, type 1. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs1567848711 linked to?

On MyGeneLog this position is linked to Neurofibromatosis, Type 1. The research behind each link, and its sources, are set out on that condition page.

Does having rs1567848711 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 rs1567848711 come from?

ClinVar VCV000804167, 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

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Neurofibromatosis, type 1 (rs1567848711). MyGeneLog™. https://www.mygenelog.com/variants/rs1567848711

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