ClinVar Miner

Submissions for variant NM_024675.4(PALB2):c.2834+13C>G

dbSNP: rs551516577
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV001187467 SCV001354285 likely benign Hereditary cancer-predisposing syndrome 2019-03-21 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002068466 SCV002411416 likely benign Familial cancer of breast 2021-10-08 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002497653 SCV002813050 likely benign Familial cancer of breast; Fanconi anemia complementation group N; Pancreatic cancer, susceptibility to, 3 2022-03-30 criteria provided, single submitter clinical testing

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