ClinVar Miner

Submissions for variant NM_005343.4(HRAS):c.425T>C (p.Ile142Thr)

dbSNP: rs2133986466
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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 RCV001871491 SCV002148714 uncertain significance Costello syndrome 2021-09-24 criteria provided, single submitter clinical testing

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