ClinVar Miner

Submissions for variant NM_001166108.2(PALLD):c.1965-12800C>T

gnomAD frequency: 0.00002  dbSNP: rs863224383
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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 RCV000199978 SCV000253363 likely benign Pancreatic adenocarcinoma 2024-01-22 criteria provided, single submitter clinical testing
KCCC/NGS Laboratory, Kuwait Cancer Control Center RCV003316105 SCV004016532 likely benign Pancreatic cancer, susceptibility to, 1 2023-07-07 criteria provided, single submitter clinical testing

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