ClinVar Miner

Submissions for variant NM_000388.4(CASR):c.1377+19T>C

dbSNP: rs2074639946
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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 RCV002041967 SCV002108520 likely benign Familial hypocalciuric hypercalcemia; Autosomal dominant hypocalcemia 1 2023-06-09 criteria provided, single submitter clinical testing

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