ClinVar Miner

Submissions for variant NM_183235.3(RAB27A):c.239+9T>C

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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 RCV003505540 SCV004249883 likely benign Griscelli syndrome type 2 2024-01-14 criteria provided, single submitter clinical testing

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