ClinVar Miner

Submissions for variant NM_021098.3(CACNA1H):c.6339C>A (p.Pro2113=)

dbSNP: rs768959857
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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 RCV000929840 SCV001075476 likely benign not provided 2018-06-20 criteria provided, single submitter clinical testing

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