ClinVar Miner

Submissions for variant NM_001166108.2(PALLD):c.1965-12953C>T

gnomAD frequency: 0.00493  dbSNP: rs528879194
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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 RCV000197834 SCV000252758 benign Pancreatic adenocarcinoma 2024-01-18 criteria provided, single submitter clinical testing
KCCC/NGS Laboratory, Kuwait Cancer Control Center RCV003316096 SCV004016528 benign Pancreatic cancer, susceptibility to, 1 2023-07-07 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004717084 SCV005303933 benign not provided criteria provided, single submitter not provided

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