ClinVar Miner

Submissions for variant NM_173689.7(CRB2):c.3262G>A (p.Gly1088Ser)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center RCV004515790 SCV005016568 likely pathogenic Focal segmental glomerulosclerosis 9 2024-03-14 criteria provided, single submitter clinical testing

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