ClinVar Miner

Submissions for variant NM_001166108.2(PALLD):c.1965-12665G>C

gnomAD frequency: 0.00111  dbSNP: rs535155432
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001083802 SCV000166476 benign Pancreatic adenocarcinoma 2024-01-18 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000123171 SCV001154311 benign not provided 2022-06-01 criteria provided, single submitter clinical testing PALLD: BS1, BS2
GeneDx RCV000123171 SCV001865357 benign not provided 2020-05-13 criteria provided, single submitter clinical testing

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