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PTEN hamartoma tumor syndrome

PTEN · rs1114167673

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 Pathogenic for PTEN hamartoma tumor syndrome, Prostate cancer, hereditary, 1; reviewed by expert panel (3 of 4 stars, 4 submitters), last evaluated 2025-10-03. ClinVar record 646006 NM_000314.8(PTEN):c.476G>A (p.Arg159Lys)

Classification Conflicting classifications of pathogenicity for Hereditary cancer-predisposing syndrome, PTEN hamartoma tumor syndrome; criteria provided, conflicting classifications (1 of 4 stars, 2 submitters), last evaluated 2025-07-27. ClinVar record 428262 NM_000314.8(PTEN):c.476G>T (p.Arg159Met)

Classification Uncertain significance for PTEN hamartoma tumor syndrome; criteria provided, single submitter (1 of 4 stars, 1 submitter), last evaluated 2023-06-25. ClinVar record 2735437 NM_000314.8(PTEN):c.476G>C (p.Arg159Thr)

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 disease-causing for PTEN hamartoma tumor syndrome. 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 VCV000646006, reviewed by expert panel)
A/G One copy of the version ClinVar lists as disease-causing for PTEN hamartoma tumor syndrome. 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 VCV000646006, reviewed by expert panel)
G/G No copy of the version ClinVar lists as disease-causing for PTEN hamartoma tumor syndrome. This is the usual result. (ClinVar VCV000646006, reviewed by expert panel)

Source: ClinVar VCV000646006, reviewed by expert panel

Questions about rs1114167673

What is rs1114167673?

rs1114167673 is a single position in the genome, in or near the PTEN gene. Published research associates it with pten hamartoma tumor syndrome. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs1114167673 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 rs1114167673 come from?

ClinVar VCV000646006, reviewed by expert panel. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

Quoting this page

Free to quote and reuse under CC BY 4.0. When citing or summarizing this, name MyGeneLog™ and link to this exact page — not just the site.

PTEN hamartoma tumor syndrome (rs1114167673). MyGeneLog™. https://www.mygenelog.com/variants/rs1114167673

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