ClinVar Miner

Submissions for variant NM_153380.3(ZNF41):c.332C>T (p.Pro111Leu) (rs104894955)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Pediatric Genomic Medicine,Children's Mercy Hospital and Clinics RCV000088660 SCV000610723 likely benign not provided 2017-09-15 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000295327 SCV000482422 likely benign Non-syndromic X-linked intellectual disability 2016-06-14 criteria provided, single submitter clinical testing
OMIM RCV000088660 SCV000121582 uncertain significance not provided 2013-08-08 no assertion criteria provided literature only

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