ClinVar Miner

Submissions for variant CASR, ALU INS, CODON 877

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000008816 SCV000029026 pathogenic Hypocalciuric hypercalcemia, familial, type 1 1997-04-15 no assertion criteria provided literature only
OMIM RCV000008817 SCV000029027 pathogenic Neonatal severe hyperparathyroidism 1997-04-15 no assertion criteria provided literature only

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