Variants studied for Alzheimer disease 9

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)

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
8	6	17	2	0	33

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	total
ABCA7	7	6	16	2	31
ABCA7, LOC130062871	0	0	1	0	1
SORL1	1	0	0	0	1

Submitter and significance breakdown #

Total submitters: 16

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	total
Neuberg Centre For Genomic Medicine, NCGM	0	0	6	0	6
Variantyx, Inc.	1	3	0	0	4
CENTOGENE GmbH and LLC - Guiding Precision Medicine	0	0	3	0	3
Kosik Lab, Neuroscience Research Institute, University of California Santa Barbara	3	0	0	0	3
Centre for Mendelian Genomics, University Medical Centre Ljubljana	0	0	2	0	2
Department of Pathology and Laboratory Medicine, Sinai Health System	0	0	2	0	2
Fulgent Genetics, Fulgent Genetics	0	0	0	2	2
Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre	0	1	1	0	2
OMIM	2	0	0	0	2
Centre for Medical Genetics, Mumbai	0	1	0	0	1
Clinical Genetics Laboratory, University Hospital Schleswig-Holstein	0	0	1	0	1
HudsonAlpha Institute for Biotechnology, HudsonAlpha Institute for Biotechnology	1	0	0	0	1
Institute of Immunology and Genetics Kaiserslautern	1	0	0	0	1
Laboratorio de Genetica e Diagnostico Molecular, Hospital Israelita Albert Einstein	0	0	1	0	1
MVZ Medizinische Genetik Mainz	0	1	0	0	1
Mendelics	0	0	1	0	1

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