ClinVar Miner

Submissions for variant NM_003072.5(SMARCA4):c.3952-9G>A

dbSNP: rs910572313
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000952634 SCV001099151 likely benign Rhabdoid tumor predisposition syndrome 2 2022-01-17 criteria provided, single submitter clinical testing
Sema4, Sema4 RCV002258072 SCV002532934 uncertain significance Hereditary cancer-predisposing syndrome 2021-12-22 criteria provided, single submitter curation

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