ClinVar Miner

Submissions for variant NM_005633.4(SOS1):c.192C>G (p.Pro64=)

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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 RCV003654562 SCV004484539 likely benign RASopathy 2023-03-21 criteria provided, single submitter clinical testing

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