ClinVar Miner

Submissions for variant NM_000059.4(BRCA2):c.691_692delinsGA (p.Ser231Asp)

dbSNP: rs2072384735
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genomic Center, National Cancer Institute RCV001310069 SCV001499592 pathogenic Familial cancer of breast no assertion criteria provided case-control

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