ClinVar Miner

Submissions for variant NM_005343.4(HRAS):c.495G>A (p.Gln165=)

dbSNP: rs2133982327
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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 RCV002218948 SCV002363370 likely benign Costello syndrome 2021-06-29 criteria provided, single submitter clinical testing

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