Sensitive

PNPT1-related disorder

PNPT1 · rs572684828

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

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 PNPT1-related disorder; criteria provided, multiple submitters, no conflicts (2 of 4 stars, 3 submitters), last evaluated 2024-07-06. ClinVar record 1199970 NM_033109.5(PNPT1):c.419C>T (p.Pro140Leu)

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 ClinVar lists as likely disease-causing for PNPT1-related disorder. 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 VCV001199970, criteria provided, multiple submitters, no conflicts)

A/G One copy of the version ClinVar lists as likely disease-causing for PNPT1-related disorder. 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 VCV001199970, criteria provided, multiple submitters, no conflicts)

G/G No copy of the version ClinVar lists as likely disease-causing for PNPT1-related disorder. This is the usual result. (ClinVar VCV001199970, criteria provided, multiple submitters, no conflicts)

Source: ClinVar VCV001199970, criteria provided, multiple submitters, no conflicts

Questions about rs572684828

What is rs572684828?

rs572684828 is a single position in the genome, in or near the PNPT1 gene. Published research associates it with pnpt1-related disorder. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs572684828 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 rs572684828 come from?

ClinVar VCV001199970, 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

PNPT1-related disorder (rs572684828). MyGeneLog™. https://www.mygenelog.com/variants/rs572684828

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