ClinVar Miner

Submissions for variant NM_002332.3(LRP1):c.1576C>G (p.Leu526Val)

dbSNP: rs770169648
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genomic Medicine Lab, University of California San Francisco RCV001007928 SCV001167639 uncertain significance Tricuspid atresia; Ventricular septal defect 2018-12-20 criteria provided, single submitter clinical testing

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