ClinVar Miner

Submissions for variant NM_183235.3(RAB27A):c.93T>C (p.Asp31=)

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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 RCV002942762 SCV003271949 likely benign Griscelli syndrome type 2 2022-02-11 criteria provided, single submitter clinical testing

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