ClinVar Miner

Submissions for variant NM_005633.4(SOS1):c.3018A>C (p.Thr1006=)

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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 RCV003655749 SCV004489298 likely benign RASopathy 2022-12-29 criteria provided, single submitter clinical testing

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