ClinVar Miner

Submissions for variant NM_001379610.1(SPINK1):c.195-21T>A

gnomAD frequency: 0.00021  dbSNP: rs377350168
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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 RCV000507485 SCV000605248 likely benign not specified 2017-01-17 criteria provided, single submitter clinical testing
KCCC/NGS Laboratory, Kuwait Cancer Control Center RCV003316660 SCV004015543 likely benign Hereditary pancreatitis 2023-07-07 criteria provided, single submitter clinical testing

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