ClinVar Miner

Submissions for variant NM_000388.4(CASR):c.1074C>T (p.Cys358=)

dbSNP: rs886044221
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000345377 SCV000343990 uncertain significance not provided 2016-07-29 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003765668 SCV004586524 likely benign Familial hypocalciuric hypercalcemia; Autosomal dominant hypocalcemia 1 2023-03-26 criteria provided, single submitter clinical testing

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