ClinVar Miner

Variants studied for Friedreich ataxia 1

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
3 0 1 1 1 6

Gene and significance breakdown #

Total genes and gene combinations: 2
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Gene or gene combination pathogenic uncertain significance likely benign benign total
FXN 2 1 1 1 5
FXN, LOC108510657 1 0 0 0 1

Submitter and significance breakdown #

Total submitters: 5
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Submitter pathogenic uncertain significance likely benign benign total
OMIM 2 0 0 0 2
Baylor Genetics 0 1 0 0 1
Institute of Human Genetics,Cologne University 1 0 0 0 1
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen 0 0 0 1 1
Institute of Genomic Medicine, Catholic University 0 0 1 0 1

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