ClinVar Miner

Submissions for variant NM_007294.4(BRCA1):c.212+21G>A

gnomAD frequency: 0.00003  dbSNP: rs80358147
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000112020 SCV000489277 likely benign Breast-ovarian cancer, familial, susceptibility to, 1 2016-09-12 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000506766 SCV000602697 likely benign not specified 2016-11-07 criteria provided, single submitter clinical testing
Breast Cancer Information Core (BIC) (BRCA1) RCV000112020 SCV000144664 uncertain significance Breast-ovarian cancer, familial, susceptibility to, 1 2006-07-19 no assertion criteria provided clinical testing

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