ClinVar Miner

Submissions for variant NM_007294.4(BRCA1):c.-19-32AT[7]

dbSNP: rs273898667
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Michigan Medical Genetics Laboratories, University of Michigan RCV000210998 SCV000267677 likely benign Breast-ovarian cancer, familial, susceptibility to, 1 2016-04-21 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001512261 SCV001719645 benign Hereditary breast ovarian cancer syndrome 2022-11-29 criteria provided, single submitter clinical testing
Sema4, Sema4 RCV002257514 SCV002538066 likely benign Hereditary cancer-predisposing syndrome 2021-05-20 criteria provided, single submitter curation
Breast Cancer Information Core (BIC) (BRCA1) RCV000210998 SCV000143938 benign Breast-ovarian cancer, familial, susceptibility to, 1 1997-11-14 no assertion criteria provided clinical testing

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