ClinVar Miner

Submissions for variant NM_000388.4(CASR):c.2583C>T (p.Leu861=)

dbSNP: rs2107650764
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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 RCV002181290 SCV002476621 likely benign Familial hypocalciuric hypercalcemia; Autosomal dominant hypocalcemia 1 2020-12-09 criteria provided, single submitter clinical testing

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