ClinVar Miner

Submissions for variant NM_005343.4(HRAS):c.291-8C>T

gnomAD frequency: 0.00003  dbSNP: rs1057522962
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000433431 SCV000530150 likely benign not provided 2020-12-01 criteria provided, single submitter clinical testing
Invitae RCV001084880 SCV001008222 likely benign Costello syndrome 2024-01-11 criteria provided, single submitter clinical testing

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