ClinVar Miner

Submissions for variant NM_001166108.2(PALLD):c.*172G>A

dbSNP: rs1762578631
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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 RCV002091462 SCV002390572 likely benign Pancreatic adenocarcinoma 2021-09-15 criteria provided, single submitter clinical testing

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