ClinVar Miner

Submissions for variant NM_007272.3(CTRC):c.40+18G>A

gnomAD frequency: 0.00001  dbSNP: rs1708076823
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV001286819 SCV001473438 likely benign Hereditary pancreatitis 2019-09-13 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001286819 SCV005823244 likely benign Hereditary pancreatitis 2024-02-20 criteria provided, single submitter clinical testing

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