ClinVar Miner

Submissions for variant NM_000059.4(BRCA2):c.3648del (p.Phe1216fs)

dbSNP: rs2072485514
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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 RCV002267159 SCV002549106 pathogenic Hereditary cancer-predisposing syndrome no assertion criteria provided case-control

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