Variants studied for Microcephaly, short stature, and impaired glucose metabolism 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
4	4	4	0	0	11

Gene and significance breakdown #

Total genes and gene combinations: 1

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Gene or gene combination	pathogenic	likely pathogenic	uncertain significance	total
TRMT10A	4	4	4	11

Submitter and significance breakdown #

Total submitters: 11

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Submitter	pathogenic	likely pathogenic	uncertain significance	total
OMIM	2	0	0	2
Baylor Genetics	0	0	2	2
MGZ Medical Genetics Center	0	2	0	2
Centogene AG - the Rare Disease Company	0	1	0	1
Fulgent Genetics, Fulgent Genetics	0	0	1	1
Foundation for Research in Genetics and Endocrinology, FRIGE's Institute of Human Genetics	1	0	0	1
Kasturba Medical College, Manipal, Kasturba Medical College, Manipal, Manipal Academy of Higher Education, Manipal, India	1	0	0	1
Institute of Human Genetics, University of Leipzig Medical Center	0	0	1	1
Institut de Recherche Interdisciplinaire en Biologie Humaine et Moleculaire, Universite Libre de Bruxelles	0	1	0	1
3billion	1	0	0	1
Pediatric Genetics Clinic, Sheba Medical Center	1	0	0	1

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