ClinVar Miner

Submissions for variant NM_004621.6(TRPC6):c.2694_2696del (p.Leu899del)

dbSNP: rs2136635187
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Human Genetics, University Hospital Muenster RCV002204556 SCV002496162 uncertain significance Focal segmental glomerulosclerosis 2 2020-04-19 criteria provided, single submitter clinical testing ACMG categories: PM2,PM4

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