Variants studied for Leydig cell hypoplasia, type 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)
		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
16	7	42	12	14	88

Gene and significance breakdown #

Total genes and gene combinations: 1

Download table as spreadsheet

Gene or gene combination	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
LHCGR, STON1-GTF2A1L	16	7	42	12	14	88

Submitter and significance breakdown #

Total submitters: 14

Download table as spreadsheet

Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
Illumina Laboratory Services, Illumina	0	0	37	12	13	62
OMIM	10	0	0	0	0	10
Fulgent Genetics, Fulgent Genetics	1	1	1	0	1	4
Clinical Molecular Genetics Laboratory, Johns Hopkins All Children's Hospital	3	0	0	0	0	3
Laboratorio de Genetica e Diagnostico Molecular, Hospital Israelita Albert Einstein	0	2	1	0	0	3
Women's Health and Genetics/Laboratory Corporation of America, LabCorp	2	0	0	0	0	2
Equipe Genetique des Anomalies du Developpement, Université de Bourgogne	0	2	0	0	0	2
Institute for Human Genetics and Genomic Medicine, Uniklinik RWTH Aachen	0	1	0	0	0	1
Medical Molecular Genetics Department, National Research Center	1	0	0	0	0	1
Magee Womens Research Institute, University of Pittsburgh Medical Center	0	1	0	0	0	1
Dr. med. U. Finckh, Human Genetics, Eurofins MVZ	0	0	1	0	0	1
Pediatric Endocrinology Clinic, Ege University School of Medicine	1	0	0	0	0	1
Neuberg Centre For Genomic Medicine, NCGM	0	0	1	0	0	1
MVZ Medizinische Genetik Mainz	0	0	1	0	0	1

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.