ClinVar Miner

Submissions for variant NM_005633.4(SOS1):c.3807A>T (p.Thr1269=)

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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 RCV002596389 SCV003504429 likely benign RASopathy 2023-03-31 criteria provided, single submitter clinical testing

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