ClinVar Miner

Submissions for variant NM_001166108.2(PALLD):c.1965-12636G>A

gnomAD frequency: 0.00160  dbSNP: rs543821321
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000123172 SCV000166477 likely benign Pancreatic adenocarcinoma 2024-01-25 criteria provided, single submitter clinical testing
GeneDx RCV000160874 SCV000211562 benign not specified 2014-01-14 criteria provided, single submitter clinical testing This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
CeGaT Center for Human Genetics Tuebingen RCV003436939 SCV004151810 benign not provided 2022-05-01 criteria provided, single submitter clinical testing PALLD: BS1, BS2

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