Variants studied for intellectual disability, X-linked, syndromic, 35

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
3	1	9	0	1	13

Gene and significance breakdown #

Total genes and gene combinations: 2

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Gene or gene combination	pathogenic	likely pathogenic	uncertain significance	benign	total
RPL10	3	1	9	0	12
LOC130068867, RPL10	0	0	0	1	1

Submitter and significance breakdown #

Total submitters: 11

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Submitter	pathogenic	likely pathogenic	uncertain significance	benign	total
OMIM	3	0	0	0	3
Baylor Genetics	0	0	2	0	2
Institute of Human Genetics, University of Goettingen	0	0	1	0	1
Care4Rare-SOLVE, CHEO	0	0	1	0	1
Foundation for Research in Genetics and Endocrinology, FRIGE's Institute of Human Genetics	0	1	0	0	1
Centre for Mendelian Genomics, University Medical Centre Ljubljana	0	0	1	0	1
Juno Genomics, Hangzhou Juno Genomics, Inc	0	0	1	0	1
Laboratory of Medical Genetics, University of Torino	0	0	1	0	1
Johns Hopkins Genomics, Johns Hopkins University	0	0	1	0	1
Genome-Nilou Lab	0	0	0	1	1
Molecular Genetics Lab, CHRU Brest	0	0	1	0	1

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