ClinVar Miner

Submissions for variant NM_000901.5(NR3C2):c.2657T>G (p.Leu886Arg)

dbSNP: rs1560928649
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Department of Pediatric Endocrinology, Cukurova University Medical Faculty RCV000761556 SCV000890144 likely pathogenic Autosomal dominant pseudohypoaldosteronism type 1 criteria provided, single submitter research

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