Variants in gene ARHGAP35

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
4	10	84	4	3	105

Condition and significance breakdown #

Total conditions: 10

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Condition	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
not specified	0	0	73	1	0	74
Martsolf syndrome 1	0	9	5	3	0	17
not provided	0	0	2	0	3	5
ARHGAP35-related condition	0	0	2	0	0	2
Neurodevelopmental disorder	1	1	0	0	0	2
Anophthalmia	0	0	1	0	0	1
Bilateral microphthalmos	1	0	0	0	0	1
Breast ductal adenocarcinoma	0	0	1	0	0	1
Irido-corneo-trabecular dysgenesis	1	0	0	0	0	1
Unilateral microphthalmos	1	0	0	0	0	1

Submitter and significance breakdown #

Total submitters: 10

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
Ambry Genetics	0	0	73	1	0	74
Reproductive Endocrine Unit, Massachusetts General Hospital	0	9	5	3	0	17
Human Developmental Genetics Laboratory, Medical College of Wisconsin	3	0	1	0	0	4
Labcorp Genetics (formerly Invitae), Labcorp	0	0	0	0	3	3
Breakthrough Genomics, Breakthrough Genomics	0	0	0	0	3	3
PreventionGenetics, part of Exact Sciences	0	0	2	0	0	2
Victorian Clinical Genetics Services, Murdoch Childrens Research Institute	1	1	0	0	0	2
Greenwood Genetic Center Diagnostic Laboratories, Greenwood Genetic Center	0	0	1	0	0	1
Mayo Clinic Laboratories, Mayo Clinic	0	0	1	0	0	1
Next Generation Diagnostics, Novartis Institutes for BioMedical Research, Inc.	0	0	1	0	0	1

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