Variants in gene ZNF536 - ClinVar Miner

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

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	109	14	7	129

Condition and significance breakdown #

Total conditions: 5

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Condition	uncertain significance	likely benign	benign	total
not specified	104	4	1	109
not provided	2	10	7	18
See cases	2	0	0	2
High myopia	1	0	0	1
Neurodevelopmental disorder	1	0	0	1

Submitter and significance breakdown #

Total submitters: 13

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Submitter	uncertain significance	likely benign	benign	total
Ambry Genetics	103	4	0	107
Labcorp Genetics (formerly Invitae), Labcorp	0	4	6	10
Breakthrough Genomics, Breakthrough Genomics	0	2	6	8
CeGaT Center for Human Genetics Tuebingen	0	6	0	6
Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine	0	0	1	1
ARUP Laboratories, Cytogenetics and Genomic Microarray, ARUP Laboratories	1	0	0	1
HudsonAlpha Institute for Biotechnology, HudsonAlpha Institute for Biotechnology	1	0	0	1
Laboratory of Molecular Genetics (Pr. Bezieau's lab), CHU de Nantes	1	0	0	1
Human Genome and Stem Cell Research Center, Department of Genetics and Evolutionary Biology, Institute of Biosciences, University of São Paulo	1	0	0	1
Centre for Mendelian Genomics, University Medical Centre Ljubljana	1	0	0	1
Laboratory of Diagnostic Genome Analysis, Leiden University Medical Center (LUMC)	1	0	0	1
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center	1	0	0	1
Institute of Human Genetics, Polish Academy of Sciences	1	0	0	1

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