ClinVar Miner

Submissions for variant NM_005633.4(SOS1):c.1113A>G (p.Glu371=)

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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 RCV003656035 SCV004457741 benign RASopathy 2023-10-24 criteria provided, single submitter clinical testing

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