ClinVar Miner

Submissions for variant NM_005343.4(HRAS):c.291-15C>A

dbSNP: rs1404106769
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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 RCV002198596 SCV002484430 likely benign Costello syndrome 2023-10-28 criteria provided, single submitter clinical testing

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