CHEK2 and Hereditary Breast Carcinoma: Association Evidence

At a glance

Association overview

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

Provenance

1 source

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

CHEK2

2 source summaries

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

Hereditary Breast Carcinoma

13 database identifiers

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

ClinVar and variant evidence

3,446 clinical variants

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

Population genetics

1 GWAS phenotype

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

Literature

195 publications

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

Provenance

13 references

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