Variants studied for Intellectual disability, X-linked 99; Intellectual disability, X-linked 99, syndromic, female-restricted

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	not provided	total
0	2	7	3	0	2	14

Gene and significance breakdown #

Total genes and gene combinations: 1

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Gene or gene combination	likely pathogenic	uncertain significance	likely benign	not provided	total
USP9X	2	7	3	2	14

Submitter and significance breakdown #

Total submitters: 6

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Submitter	likely pathogenic	uncertain significance	likely benign	not provided	total
Fulgent Genetics, Fulgent Genetics	0	4	1	0	5
New York Genome Center	1	2	0	0	3
Department of Pathology and Laboratory Medicine, Sinai Health System	0	1	1	0	2
GenomeConnect - Brain Gene Registry	0	0	0	2	2
Génétique des Maladies du Développement, Hospices Civils de Lyon	1	0	0	0	1
3billion	0	0	1	0	1

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