ClinVar Miner

Submissions for variant NM_007272.3(CTRC):c.40+10G>A

gnomAD frequency: 0.00008  dbSNP: rs564455614
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002097806 SCV002386954 likely benign Hereditary pancreatitis 2024-12-18 criteria provided, single submitter clinical testing

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