ClinVar Miner

Submissions for variant NM_007294.4(BRCA1):c.4186-11C>T

gnomAD frequency: 0.00004  dbSNP: rs80358080
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV000775145 SCV000909273 likely benign Hereditary cancer-predisposing syndrome 2017-12-19 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001459035 SCV001662868 likely benign Hereditary breast ovarian cancer syndrome 2023-10-30 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV000112288 SCV004830873 likely benign Breast-ovarian cancer, familial, susceptibility to, 1 2023-12-01 criteria provided, single submitter clinical testing
Breast Cancer Information Core (BIC) (BRCA1) RCV000112288 SCV000145020 uncertain significance Breast-ovarian cancer, familial, susceptibility to, 1 2003-12-23 no assertion criteria provided clinical testing

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