ClinVar Miner

Submissions for variant NM_002769.5(PRSS1):c.540C>T (p.Thr180=)

dbSNP: rs769319141
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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 RCV001494273 SCV001698925 likely benign Hereditary pancreatitis 2018-02-25 criteria provided, single submitter clinical testing

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