ClinVar Miner

Submissions for variant NM_001128849.2(SMARCA4):c.2637T>C (p.Ile879=) (rs369795542)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000565238 SCV000664059 likely benign Hereditary cancer-predisposing syndrome 2015-07-03 criteria provided, single submitter clinical testing
Invitae RCV000230327 SCV000286027 likely benign Rhabdoid tumor predisposition syndrome 2 2017-11-27 criteria provided, single submitter clinical testing

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