ClinVar Miner

Variants in gene ZNF41

Minimum submission review status: Collection method:
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Gene type:
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If a variant has more than one submission, it may be counted in more than one significance column. If this is the case, the total number of variants will be less than the sum of the other cells.

pathogenic likely pathogenic uncertain significance likely benign benign total
0 0 71 23 11 94

Condition and significance breakdown #

Total conditions: 8
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Condition uncertain significance likely benign benign total
not specified 54 9 8 69
not provided 11 12 9 28
ZNF41-related disorder 2 3 1 6
History of neurodevelopmental disorder 2 0 3 5
See cases 2 1 0 3
Non-syndromic X-linked intellectual disability 2 0 0 2
Abnormality of neuronal migration 0 0 1 1
Global developmental delay; Seizure; Intellectual disability 1 0 0 1

Submitter and significance breakdown #

Total submitters: 18
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Submitter uncertain significance likely benign benign total
Ambry Genetics 56 7 10 73
Breakthrough Genomics, Breakthrough Genomics 2 0 9 11
CeGaT Center for Human Genetics Tuebingen 1 7 0 8
PreventionGenetics, part of Exact Sciences 2 3 1 6
Laboratory of Diagnostic Genome Analysis, Leiden University Medical Center (LUMC) 0 5 0 5
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center 0 4 1 5
Eurofins Ntd Llc (ga) 2 0 2 4
Revvity Omics, Revvity 3 0 0 3
OMIM 2 0 0 2
Genetic Services Laboratory, University of Chicago 0 2 0 2
Illumina Laboratory Services, Illumina 2 0 0 2
ISCA site 4 2 0 0 2
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen 0 2 0 2
Department of Clinical Genetics, Copenhagen University Hospital, Rigshospitalet 1 0 0 1
ISCA site 1 0 1 0 1
Génétique et pathophysiologie de maladies neurodéveloppementales et épileptogènes, Institut de génétique et de biologie moléculaire et cellulaire 0 0 1 1
Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics 0 1 0 1
Clinical Genetics Laboratory, Skane University Hospital Lund 1 0 0 1

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