BRCA2 · rs81002897
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
ClinVar classifies it as disease-causing (or likely), reviewed at 2 of 4 stars.
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 Fanconi anemia complementation group D1, Hereditary breast ovarian cancer syndrome, Breast-ovarian cancer, familial, susceptibility to, 2, Hereditary cancer-predisposing syndrome, Breast-ovarian cancer, familial, susceptibility to, 1; criteria provided, multiple submitters, no conflicts (2 of 4 stars, 11 submitters), last evaluated 2025-12-02.
ClinVar record 9348 NM_000059.4(BRCA2):c.631+1G>A
Classification
Pathogenic/Likely pathogenic for Hereditary cancer-predisposing syndrome, Breast-ovarian cancer, familial, susceptibility to, 2, Hereditary breast ovarian cancer syndrome; criteria provided, multiple submitters, no conflicts (2 of 4 stars, 4 submitters), last evaluated 2025-09-26.
ClinVar record 422774 NM_000059.4(BRCA2):c.631+1G>C
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.
Source: ClinVar VCV000009348, criteria provided, multiple submitters, no conflicts
rs81002897 is a single position in the genome, in or near the BRCA2 gene. Published research associates it with fanconi anemia complementation group d1. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
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.
ClinVar VCV000009348, 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.
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Fanconi anemia complementation group D1 (rs81002897). MyGeneLog™. https://www.mygenelog.com/variants/rs81002897