ClinVar Miner

Submissions for variant NM_001166108.2(PALLD):c.*100A>G

gnomAD frequency: 0.00001  dbSNP: rs754444061
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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 RCV002121439 SCV002449213 likely benign Pancreatic adenocarcinoma 2021-06-24 criteria provided, single submitter clinical testing

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