Variants studied for Autism, susceptibility to, X-linked 1

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)

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
2	5	8	0	1	16

Gene and significance breakdown #

Total genes and gene combinations: 1

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Gene or gene combination	pathogenic	likely pathogenic	uncertain significance	benign	total
NLGN3	2	5	8	1	16

Submitter and significance breakdown #

Total submitters: 16

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Submitter	pathogenic	likely pathogenic	uncertain significance	benign	total
3billion	0	1	0	0	1
Baylor Genetics	0	0	1	0	1
Centre for Mendelian Genomics, University Medical Centre Ljubljana	0	0	0	1	1
Clinical Genetics Laboratory, University Hospital Schleswig-Holstein	0	1	0	0	1
Department of Genetics, Sultan Qaboos University Hospital	0	0	1	0	1
Equipe Genetique des Anomalies du Developpement, Université de Bourgogne	0	0	1	0	1
Foundation for Research in Genetics and Endocrinology, FRIGE's Institute of Human Genetics	0	1	0	0	1
Institute of Human Genetics, Cologne University	0	1	0	0	1
Institute of Human Genetics, University of Leipzig Medical Center	0	0	1	0	1
Juno Genomics, Hangzhou Juno Genomics, Inc	0	0	1	0	1
MVZ Martinsried, Medicover Genetics	0	0	1	0	1
Medical Genetics Center, Maternal and Child Health Hospital of Hubei Province	0	1	0	0	1
Molecular and Human Genetics, Karnataka Institute for DNA Research	1	0	0	0	1
New York Genome Center	0	0	1	0	1
OMIM	1	0	0	0	1
Pittsburgh Clinical Genomics Laboratory, University of Pittsburgh Medical Center	0	0	1	0	1

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