ClinVar Miner

Submissions for variant NM_000059.4(BRCA2):c.7873A>C (p.Arg2625=)

dbSNP: rs2137577004
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Quest Diagnostics Nichols Institute San Juan Capistrano RCV001801130 SCV002046970 uncertain significance not provided 2021-04-22 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV005095176 SCV005819380 likely benign Hereditary breast ovarian cancer syndrome 2024-08-03 criteria provided, single submitter clinical testing

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