Standard

Pulmonary hypertension, primary, 1

BMPR2 · rs368090069

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

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 Pulmonary hypertension, primary, 1, Primary pulmonary hypertension; criteria provided, conflicting classifications (1 of 4 stars, 3 submitters), last evaluated 2025-12-13. ClinVar record 896821 NM_001204.7(BMPR2):c.248-3T>C

Classification Pathogenic for Pulmonary hypertension, primary, 1; no assertion criteria provided (0 of 4 stars, 1 submitter). ClinVar record 425736 NM_001204.7(BMPR2):c.248-3T>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

G/G Two copies of the version ClinVar lists as disease-causing for Pulmonary hypertension, primary, 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. This call was sent to ClinVar without the lab's criteria, the least certain kind of record, so it may change. (ClinVar VCV000425736, no assertion criteria provided)

G/T One copy of the version ClinVar lists as disease-causing for Pulmonary hypertension, primary, 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. This call was sent to ClinVar without the lab's criteria, the least certain kind of record, so it may change. (ClinVar VCV000425736, no assertion criteria provided)

T/T No copy of the version ClinVar lists as disease-causing for Pulmonary hypertension, primary, 1. This is the usual result. This call was sent to ClinVar without the lab's criteria, the least certain kind of record, so it may change. (ClinVar VCV000425736, no assertion criteria provided)

Source: ClinVar VCV000425736, no assertion criteria provided

Questions about rs368090069

What is rs368090069?

rs368090069 is a single position in the genome, in or near the BMPR2 gene. Published research associates it with pulmonary hypertension, primary, 1. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs368090069 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 rs368090069 come from?

ClinVar VCV000425736, no assertion criteria provided. 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.

Pulmonary hypertension, primary, 1 (rs368090069). MyGeneLog™. https://www.mygenelog.com/variants/rs368090069

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