ClinVar Miner

Submissions for variant NM_007373.4(SHOC2):c.1285-5A>C

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003654869 SCV004550900 likely benign RASopathy 2023-03-31 criteria provided, single submitter clinical testing

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