Variants studied for KINSSHIP syndrome

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
7	4	9	1	2	22

Gene and significance breakdown #

Total genes and gene combinations: 1

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Gene or gene combination	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
AFF3	7	4	9	1	2	22

Submitter and significance breakdown #

Total submitters: 14

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
OMIM	6	0	0	0	0	6
Neuberg Centre For Genomic Medicine, NCGM	0	0	3	0	0	3
Baylor Genetics	0	0	2	0	0	2
Fulgent Genetics, Fulgent Genetics	0	1	0	0	1	2
Revvity Omics, Revvity	0	0	1	0	0	1
MGZ Medical Genetics Center	0	0	1	0	0	1
Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre	0	0	0	1	0	1
Institute of Human Genetics, FAU Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg	0	1	0	0	0	1
HudsonAlpha Institute for Biotechnology, HudsonAlpha Institute for Biotechnology	0	0	1	0	0	1
Laboratory of Medical Genetics, National & Kapodistrian University of Athens	1	0	0	0	0	1
Laboratory of Medical Genetics, University of Torino	0	1	0	0	0	1
New York Genome Center	0	0	1	0	0	1
3billion	0	1	0	0	0	1
Molecular Genetics, Royal Melbourne Hospital	0	0	0	0	1	1

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