ClinVar Miner

Variants studied for amyotrophic lateral sclerosis type 9

Included ClinVar conditions (1):
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 2 16 8 13 43

Gene and significance breakdown #

Total genes and gene combinations: 5
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Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign benign total
ANG, EGILA, RNASE4 10 2 10 7 4 27
ANG 0 0 3 0 5 8
ANG, LOC130055269 0 0 1 0 3 4
ANG, LOC130055270, RNASE4 0 0 0 1 1 2
ANG, RNASE4 0 0 2 0 0 2

Submitter and significance breakdown #

Total submitters: 7
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign total
Illumina Laboratory Services, Illumina 0 0 13 8 13 34
OMIM 10 0 0 0 0 10
Mendelics 0 0 1 0 1 2
Revvity Omics, Revvity 0 0 1 0 0 1
Women's Health and Genetics/Laboratory Corporation of America, LabCorp 0 1 0 0 0 1
Institute of Medical Genetics and Applied Genomics, University Hospital Tübingen 0 1 0 0 0 1
Suna and Inan Kirac Foundation Neurodegeneration Research Laboratory, Koc University 0 0 1 0 0 1

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