ClinVar Miner

Submissions for variant NM_000388.4(CASR):c.-378del

dbSNP: rs537119483
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000314365 SCV000484008 likely benign Familial hypoparathyroidism 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000345882 SCV000484009 likely benign Hypocalcemia 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000395625 SCV000484010 likely benign Familial hypocalciuric hypercalcemia 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000310837 SCV000484011 likely benign Neonatal severe primary hyperparathyroidism 2016-06-14 criteria provided, single submitter clinical testing

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