ClinVar Miner

Submissions for variant NM_005343.4(HRAS):c.111+17C>T

gnomAD frequency: 0.00001  dbSNP: rs1851313358
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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 RCV002202177 SCV002355270 likely benign Costello syndrome 2023-08-11 criteria provided, single submitter clinical testing

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