ClinVar Miner

Submissions for variant NM_005343.4(HRAS):c.451-12C>T

dbSNP: rs1204923566
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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 RCV002217118 SCV002364190 likely benign Costello syndrome 2023-11-18 criteria provided, single submitter clinical testing

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