Variants studied for Fibrochondrogenesis 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
3	1	131	19	45	198

Gene and significance breakdown #

Total genes and gene combinations: 3

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Gene or gene combination	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
COL11A1	3	1	126	15	44	188
COL11A2	0	0	1	4	1	6
COL11A1, LOC126805814	0	0	4	0	0	4

Submitter and significance breakdown #

Total submitters: 8

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
Illumina Laboratory Services, Illumina	0	0	123	19	36	178
Genome-Nilou Lab	0	0	0	0	16	16
Baylor Genetics	1	0	4	0	0	5
Mendelics	2	0	1	0	2	5
3billion	0	1	2	0	0	3
Victorian Clinical Genetics Services, Murdoch Childrens Research Institute	0	0	1	0	0	1
Genomic Research Center, Shahid Beheshti University of Medical Sciences	0	0	1	0	0	1
Molecular Genetics, Royal Melbourne Hospital	0	0	0	0	1	1

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