ClinVar Miner

Submissions for variant NM_001324144.2(ZNF41):c.332C>T (p.Pro111Leu)

gnomAD frequency: 0.00065  dbSNP: 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
CeGaT Center for Human Genetics Tuebingen RCV000088660 SCV004700371 likely benign not provided 2024-04-01 criteria provided, single submitter clinical testing ZNF41: BP4, BS2
OMIM RCV000088660 SCV000121582 uncertain significance not provided 2013-08-08 no assertion criteria provided literature only

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