ClinVar Miner

Submissions for variant NM_007272.3(CTRC):c.231-14C>T

gnomAD frequency: 0.00046  dbSNP: rs374364850
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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 RCV001001717 SCV001159302 likely benign Hereditary pancreatitis 2019-01-25 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001001717 SCV002407490 benign Hereditary pancreatitis 2024-01-09 criteria provided, single submitter clinical testing

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