ClinVar Miner

Submissions for variant NM_000388.4(CASR):c.*188dup

dbSNP: rs33974189
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000319534 SCV000440167 benign Neonatal severe primary hyperparathyroidism 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000355280 SCV000440168 benign Familial hypoparathyroidism 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000260384 SCV000440169 benign Familial hypocalciuric hypercalcemia 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000315706 SCV000440170 benign Hypocalcemia 2016-06-14 criteria provided, single submitter clinical testing

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