ClinVar Miner

Variants studied for amyotrophic lateral sclerosis type 4

Included ClinVar conditions (2):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
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
10 3 306 112 79 485

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
SETX 10 3 306 112 79 485

Submitter and significance breakdown #

Total submitters: 13
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign total
Invitae 6 1 208 88 30 333
Illumina Clinical Services Laboratory,Illumina 0 0 102 32 58 192
Fulgent Genetics,Fulgent Genetics 0 0 8 0 0 8
Mendelics 1 2 0 0 3 6
OMIM 3 0 0 0 0 3
Baylor Genetics 0 0 3 0 0 3
Athena Diagnostics Inc 0 0 0 0 2 2
Genomic Research Center, Shahid Beheshti University of Medical Sciences 0 0 2 0 0 2
Institute of Human Genetics,Cologne University 0 0 1 0 0 1
Northcott Neuroscience Laboratory, ANZAC Research Institute 1 0 0 0 0 1
Knight Diagnostic Laboratories, Oregon Health and Sciences University 0 0 1 0 0 1
Suna and Inan Kirac Foundation Neurodegeneration Research Laboratory, Koc University 0 0 1 0 0 1
Paris Brain Institute,Inserm - ICM 1 0 0 0 0 1

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