ClinVar Miner

Submissions for variant NM_173689.7(CRB2):c.1827C>A (p.Cys609Ter)

dbSNP: rs1388484958
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Molecular Biology Laboratory, Fundació Puigvert RCV001281246 SCV001425070 pathogenic Focal segmental glomerulosclerosis 9 2020-02-01 criteria provided, single submitter research

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