ClinVar Miner

Submissions for variant NM_000059.4(BRCA2):c.4948del (p.Ser1650fs)

dbSNP: rs80359474
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genomic Center, National Cancer Institute RCV002267165 SCV002549112 pathogenic Hereditary cancer-predisposing syndrome no assertion criteria provided case-control
Laboratory for Genotyping Development, RIKEN RCV003164391 SCV002758429 pathogenic Gastric cancer 2021-07-01 no assertion criteria provided research

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