ClinVar Miner

Submissions for variant NM_183235.3(RAB27A):c.174G>A (p.Pro58=)

dbSNP: rs910190895
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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 RCV001460429 SCV001664300 likely benign Griscelli syndrome type 2 2022-10-27 criteria provided, single submitter clinical testing

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