ClinVar Miner

Submissions for variant NM_000059.4(BRCA2):c.8573A>C (p.Gln2858Pro)

dbSNP: rs80359114
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Quest Diagnostics Nichols Institute San Juan Capistrano RCV001284450 SCV001470254 uncertain significance not provided 2019-09-17 criteria provided, single submitter clinical testing

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