ClinVar Miner

Variants studied for Spinocerebellar ataxia 44

Coded as:
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
3 0 5 0 5 13

Gene and significance breakdown #

Total genes and gene combinations: 1
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Gene or gene combination pathogenic uncertain significance benign total
GRM1 3 5 5 13

Submitter and significance breakdown #

Total submitters: 6
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Submitter pathogenic uncertain significance benign total
Genome-Nilou Lab 0 0 5 5
OMIM 3 0 0 3
Baylor Genetics 0 2 0 2
O&I group, Department of Genetics, University Medical Center of Groningen 1 1 0 2
Genetics and Molecular Pathology, SA Pathology 0 1 0 1
Diagnostics Services (NGS), CSIR - Centre For Cellular And Molecular Biology 0 1 0 1

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