ClinVar Miner

Submissions for variant NM_000059.4(BRCA2):c.4284del (p.Gln1429fs)

dbSNP: rs80359439
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Human Genetics, University of Wuerzburg RCV000678455 SCV000804518 pathogenic Ovarian neoplasm no assertion criteria provided clinical testing
Genomic Center, National Cancer Institute RCV001310071 SCV001499594 pathogenic Familial cancer of breast no assertion criteria provided case-control

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