ClinVar Miner

Submissions for variant NM_005343.4(HRAS):c.177C>G (p.Ala59=)

dbSNP: rs730880456
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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 RCV001457720 SCV001661525 likely benign Costello syndrome 2023-12-08 criteria provided, single submitter clinical testing

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