ClinVar Miner

Submissions for variant NM_001166108.2(PALLD):c.1965-12764G>C

dbSNP: rs863224384
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000196732 SCV000253364 benign Pancreatic adenocarcinoma 2023-09-10 criteria provided, single submitter clinical testing
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen RCV001795323 SCV002035057 likely benign not provided no assertion criteria provided clinical testing
Laboratory of Diagnostic Genome Analysis, Leiden University Medical Center (LUMC) RCV001795324 SCV002036503 benign not specified no assertion criteria provided clinical testing

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