ClinVar Miner

Submissions for variant NM_007373.4(SHOC2):c.1485T>C (p.Asn495=)

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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 RCV002880616 SCV003231801 likely benign RASopathy 2023-03-16 criteria provided, single submitter clinical testing

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