ClinVar Miner

Submissions for variant NM_001166108.2(PALLD):c.2199+8G>A

gnomAD frequency: 0.00070  dbSNP: rs200060953
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001083018 SCV000166482 benign Pancreatic adenocarcinoma 2024-01-28 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000310521 SCV000448485 likely benign Pancreatic cancer, susceptibility to, 1 2017-04-27 criteria provided, single submitter clinical testing This variant was observed as part of a predisposition screen in an ostensibly healthy population. A literature search was performed for the gene, cDNA change, and amino acid change (where applicable). No publications were found based on this search. Allele frequency data from public databases allowed determination this variant is unlikely to cause disease. Therefore, this variant is classified as likely benign.
CeGaT Center for Human Genetics Tuebingen RCV003389731 SCV001154315 benign not provided 2023-07-01 criteria provided, single submitter clinical testing PALLD: BS1, BS2
KCCC/NGS Laboratory, Kuwait Cancer Control Center RCV000310521 SCV004016521 benign Pancreatic cancer, susceptibility to, 1 2023-07-07 criteria provided, single submitter clinical testing

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