ClinVar Miner

Submissions for variant NM_001166108.2(PALLD):c.1965-12736A>C

dbSNP: rs864622226
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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 RCV001516271 SCV001724532 benign Pancreatic adenocarcinoma 2015-10-30 criteria provided, single submitter clinical testing

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