Genopathy
Gene-Disorder Association · Article
Gene
BRCA2
BRCA2 DNA Repair Associated
Disorder
Breast-Ovarian Cancer, Familial 2
First reported 2022
Supporting publications 695
Key publication · gene–disorder A comprehensive reference for BRCA1/2 genes pathogenic variants in Iran: published, unpublished and novel.Familial cancer · 2022
Key publication · disorder [Reactivity of anti-human bladder cancer monoclonal antibodies with bladder tumor tissues].Nihon Hinyokika Gakkai zasshi. The japanese journal of urology · 1986
Manually curated
Association Review

In brief

The association between BRCA2 (BRCA2 DNA Repair Associated) and Breast-Ovarian Cancer, Familial 2 is well established and manually curated, with its 3 contributing sources — 2 of them expert-curated — recording a known molecular basis, pathogenic variants, and a susceptibility locus.

Sources 3
Clinical variants 7,535
Symptoms 4
Compounds 0
Trials 0
Publications 695
01
At a glance

Association overview

A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.

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02
Provenance

Evidence and sources

3 sources

Every contributing database and publication behind this association, with evidence type, strength, accessions and deep links.

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03
BRCA2

The gene

2 source summaries

A gene summary alongside the source descriptions it was distilled from.

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04
Breast-Ovarian Cancer, Familial 2

The disorder

8 database identifiers

The disorder’s summary, prevalence, aliases and cross-reference identifiers (OMIM, Orphanet, MONDO, ICD-10, MedGen).

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05
Phenotype

Clinical features

2 clinical features

The disorder’s clinical features (HPO) grouped by body system, each with observed frequency and penetrance.

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06
ClinVar and variant evidence

Genetic basis

7,535 clinical variants

ClinVar variants reported for this pair, with disorder-specific significance, review status, molecular consequence and origin.

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07
Population genetics

GWAS signals

1 GWAS phenotype

Gene-associated GWAS phenotypes matching the disorder, with best SNP, score, risk-allele frequency and effect size.

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08
Mechanism overlap

Shared mechanisms

Biological pathways and phenotype concepts shared by the gene and the disorder, with supporting publications.

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09
Literature

Reading

695 publications

Publications linking the gene and the disorder, with title, authors, journal, year and citation metrics.

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10
Provenance

References & sources

15 references

Every source and publication cited across this dossier, as one numbered reference list.

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