ClinVar Miner

Submissions for variant NM_003384.3(VRK1):c.804T>G (p.Pro268=)

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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 RCV003057186 SCV003338946 likely benign Pontocerebellar hypoplasia type 1A 2022-04-11 criteria provided, single submitter clinical testing

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