ClinVar Miner

Submissions for variant NM_001166108.2(PALLD):c.1965-12908G>A

gnomAD frequency: 0.00107  dbSNP: rs758706279
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000196136 SCV000253361 likely benign Pancreatic adenocarcinoma 2023-06-23 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV003947653 SCV004760245 benign PALLD-related disorder 2019-10-10 no assertion criteria provided clinical testing This variant is classified as benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications).

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