Variants studied for Finnish type amyloidosis

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	3	155	52	44	247

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
GSN	8	3	155	52	44	247

Submitter and significance breakdown #

Total submitters: 18

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
Fulgent Genetics, Fulgent Genetics	2	0	129	44	0	175
Illumina Laboratory Services, Illumina	0	0	24	8	42	74
OMIM	4	0	0	0	0	4
Genome-Nilou Lab	0	0	0	0	3	3
3billion	1	1	0	0	0	2
Department of Pathology and Laboratory Medicine, Sinai Health System	0	0	2	0	0	2
Department of Traditional Chinese Medicine, Fujian Provincial Hospital	2	0	0	0	0	2
Genetics and Molecular Pathology, SA Pathology	1	0	1	0	0	2
Institute of Human Genetics Munich, TUM University Hospital	2	0	0	0	0	2
Revvity Omics, Revvity	0	0	2	0	0	2
Amyloidosis Center, Boston University School of Medicine	1	0	0	0	0	1
Baylor Genetics	0	0	1	0	0	1
Centre for Mendelian Genomics, University Medical Centre Ljubljana	0	0	1	0	0	1
Department of Ophthalmology, Flinders Medical Centre	0	0	1	0	0	1
Human Genome Lab, NIMHANS, National Institute of Mental Health and Neuro Sciences	0	1	0	0	0	1
Lifecell International Pvt. Ltd	0	1	0	0	0	1
Neuberg Centre For Genomic Medicine, NCGM	0	0	1	0	0	1
New York Genome Center	0	0	1	0	0	1

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