ClinVar Miner

Submissions for variant NM_024675.4(PALB2):c.3350+16T>G

gnomAD frequency: 0.00001  dbSNP: rs515726115
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV000581930 SCV000690911 likely benign Hereditary cancer-predisposing syndrome 2017-10-27 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001030412 SCV002432258 likely benign Familial cancer of breast 2023-02-26 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002498489 SCV002806731 likely benign Familial cancer of breast; Fanconi anemia complementation group N; Pancreatic cancer, susceptibility to, 3 2021-12-13 criteria provided, single submitter clinical testing
Leiden Open Variation Database RCV001030412 SCV001193399 likely benign Familial cancer of breast 2019-05-13 no assertion criteria provided curation Curators: Marc Tischkowitz, Arleen D. Auerbach. Submitter to LOVD: Marc Tischkowitz.

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