ClinVar Miner

Submissions for variant NM_004621.6(TRPC6):c.2641G>T (p.Glu881Ter)

dbSNP: rs1858816107
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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 RCV001281329 SCV001425270 likely pathogenic Focal segmental glomerulosclerosis 2 2020-02-01 criteria provided, single submitter research

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