ClinVar Miner

Submissions for variant NM_024675.4(PALB2):c.168T>C (p.Asp56=)

dbSNP: rs1203135643
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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 RCV000773731 SCV000907431 likely benign Hereditary cancer-predisposing syndrome 2018-08-14 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001465989 SCV001669988 likely benign Familial cancer of breast 2025-02-02 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002507341 SCV002797241 likely benign Familial cancer of breast; Fanconi anemia complementation group N; Pancreatic cancer, susceptibility to, 3 2022-04-05 criteria provided, single submitter clinical testing

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