ClinVar Miner

Submissions for variant NM_005343.4(HRAS):c.243G>A (p.Val81=)

dbSNP: rs2133990247
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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 RCV002586862 SCV002943091 likely benign Costello syndrome 2024-12-11 criteria provided, single submitter clinical testing

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