ClinVar Miner

Submissions for variant NM_032043.3(BRIP1):c.2085G>A (p.Leu695=)

dbSNP: rs1555601008
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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 RCV000636208 SCV000757640 likely benign Familial cancer of breast; Fanconi anemia complementation group J 2017-12-27 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV001182090 SCV001347440 likely benign Hereditary cancer-predisposing syndrome 2019-03-28 criteria provided, single submitter clinical testing

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