ClinVar Miner

Submissions for variant NM_007272.3(CTRC):c.640-35G>T

gnomAD frequency: 0.34421  dbSNP: rs10927786
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000505864 SCV000603243 benign Hereditary pancreatitis 2020-04-20 criteria provided, single submitter clinical testing
GeneDx RCV001613328 SCV001838975 benign not provided 2018-06-21 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001613328 SCV005282545 benign not provided criteria provided, single submitter not provided

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