SMARCB1 and Rhabdoid Tumor Predisposition Syndrome: Association Evidence

In brief

The association between SMARCB1 (SWI/SNF Related BAF Chromatin Remodeling Complex Subunit B1) and Rhabdoid Tumor Predisposition Syndrome is well established and manually curated, with its 3 contributing sources — 2 of them expert-curated — recording pathogenic variants and a causative germline mutation.

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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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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SMARCB1

The gene

1 source summary

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

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Rhabdoid Tumor Predisposition Syndrome

The disorder

7 database identifiers

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

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ClinVar and variant evidence

Genetic basis

82 clinical variants

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

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Literature

Reading

6 publications

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

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Provenance

References & sources

11 references

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

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