ClinVar Miner

Submissions for variant NM_003619.4(PRSS12):c.1490-7G>A

gnomAD frequency: 0.00250  dbSNP: rs183541303
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000195283 SCV000248605 likely benign not specified 2015-08-05 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000956249 SCV001102996 benign not provided 2019-12-31 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000956249 SCV004148780 likely benign not provided 2022-10-01 criteria provided, single submitter clinical testing PRSS12: BP4, BS2

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