Variants studied for Fanconi anemia complementation group N

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
29	5	60	16	7	117

Gene and significance breakdown #

Total genes and gene combinations: 2

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Gene or gene combination	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
PALB2	28	5	60	16	7	116
DCTN5, PALB2	1	0	0	0	0	1

Submitter and significance breakdown #

Total submitters: 17

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
Illumina Laboratory Services, Illumina	0	0	45	16	7	68
Revvity Omics, Revvity	17	2	8	0	0	27
Baylor Genetics	1	0	5	0	0	6
Leiden Open Variation Database	6	0	0	0	0	6
OMIM	5	0	0	0	0	5
Neuberg Centre For Genomic Medicine, NCGM	0	1	1	0	0	2
Genetic Services Laboratory, University of Chicago	1	0	0	0	0	1
MGZ Medical Genetics Center	1	0	0	0	0	1
Victorian Clinical Genetics Services, Murdoch Childrens Research Institute	1	0	0	0	0	1
HudsonAlpha Institute for Biotechnology, HudsonAlpha Institute for Biotechnology	1	0	0	0	0	1
Genetics and Molecular Pathology, SA Pathology	0	0	1	0	0	1
Department of Pathology and Laboratory Medicine, Sinai Health System	0	0	0	1	0	1
Laboratory of Functional Genomics, Research Centre for Medical Genetics	1	0	0	0	0	1
St. Jude Molecular Pathology, St. Jude Children's Research Hospital	0	0	1	0	0	1
DASA	1	0	0	0	0	1
Laboratorio de Genetica e Diagnostico Molecular, Hospital Israelita Albert Einstein	0	1	0	0	0	1
Solve-RD Consortium	0	1	0	0	0	1

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