ClinVar Miner

Submissions for variant NM_007272.3(CTRC):c.493+51C>A

gnomAD frequency: 0.21273  dbSNP: rs10803384
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000507213 SCV000603247 benign Hereditary pancreatitis 2020-02-21 criteria provided, single submitter clinical testing
GeneDx RCV001672816 SCV001884002 benign not provided 2018-06-21 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001672816 SCV005282541 benign not provided criteria provided, single submitter not provided

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