ClinVar Miner

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

dbSNP: rs1589789708
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000874555 SCV001016746 likely benign Costello syndrome 2021-12-23 criteria provided, single submitter clinical testing
Service de Génétique Moléculaire, Hôpital Robert Debré RCV000824933 SCV000965967 likely benign Noonan syndrome no assertion criteria provided clinical testing

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