ClinVar Miner

Submissions for variant NM_005343.4(HRAS):c.474G>C (p.Thr158=)

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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 RCV003626581 SCV004509366 likely benign Costello syndrome 2022-11-09 criteria provided, single submitter clinical testing

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