ClinVar Miner

Submissions for variant NM_183235.3(RAB27A):c.438G>A (p.Glu146=)

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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 RCV005088775 SCV005720685 likely benign Griscelli syndrome type 2 2024-10-28 criteria provided, single submitter clinical testing

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