ClinVar Miner

Submissions for variant NM_007294.4(BRCA1):c.*528G>C

dbSNP: rs1060504556
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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 RCV000458128 SCV000560206 likely benign Hereditary breast ovarian cancer syndrome 2021-05-03 criteria provided, single submitter clinical testing
Department of Pathology and Laboratory Medicine, Sinai Health System RCV005355896 SCV005914862 likely pathogenic Fanconi anemia, complementation group S criteria provided, single submitter clinical testing

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