ClinVar Miner

Submissions for variant NM_000059.4(BRCA2):c.2142A>G (p.Glu714=)

dbSNP: rs1593896191
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 RCV000985471 SCV001133701 uncertain significance not provided 2018-10-16 criteria provided, single submitter clinical testing

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