Variants in gene ARHGAP6

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	69	17	10	94

Condition and significance breakdown #

Total conditions: 4

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Condition	uncertain significance	likely benign	benign	total
not specified	66	0	1	67
not provided	2	16	9	27
Neurodevelopmental disorder	1	1	0	2
ARHGAP6-related disorder	0	1	0	1

Submitter and significance breakdown #

Total submitters: 11

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Submitter	uncertain significance	likely benign	benign	total
Ambry Genetics	66	0	0	66
Labcorp Genetics (formerly Invitae), Labcorp	0	10	9	19
Breakthrough Genomics, Breakthrough Genomics	0	2	5	7
CeGaT Center for Human Genetics Tuebingen	0	6	0	6
Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine	0	0	1	1
PreventionGenetics, part of Exact Sciences	0	1	0	1
Richard Lifton Laboratory, Yale University School of Medicine	1	0	0	1
Institute of Human Genetics, University of Leipzig Medical Center	0	1	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
Broad Center for Mendelian Genomics, Broad Institute of MIT and Harvard	1	0	0	1

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