ClinVar Miner

Submissions for variant NM_007272.3(CTRC):c.357-44C>G

gnomAD frequency: 0.00093  dbSNP: rs200242846
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV001001996 SCV001159810 benign Hereditary pancreatitis 2018-07-06 criteria provided, single submitter clinical testing

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