ClinVar Miner

Submissions for variant NM_001166108.2(PALLD):c.2101-9G>A

gnomAD frequency: 0.00019  dbSNP: rs368890611
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000123176 SCV000166481 likely benign Pancreatic adenocarcinoma 2023-07-14 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV003905178 SCV004726009 likely benign PALLD-related disorder 2021-11-08 criteria provided, single submitter clinical testing This variant is classified as likely benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications).

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