ClinVar Miner

Submissions for variant NM_015135.3(NUP205):c.2068G>A (p.Glu690Lys)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Pediatric/Medical Genetics, Ministry of Health, Qatif Central Hospital RCV003149169 SCV003836807 uncertain significance Nephrotic syndrome, type 13 criteria provided, single submitter clinical testing

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