ClinVar Miner

Submissions for variant NM_007294.4(BRCA1):c.3027A>C (p.Ser1009=)

dbSNP: rs1555588512
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000558515 SCV000635881 likely benign Hereditary breast ovarian cancer syndrome 2022-06-20 criteria provided, single submitter clinical testing
Liquid Biopsy and Cancer Interception Group, Pfizer-University of Granada-Junta de Andalucía Centre for Genomics and Oncological Research RCV001090202 SCV001245500 uncertain significance Breast-ovarian cancer, familial, susceptibility to, 2 criteria provided, single submitter clinical testing

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