ClinVar Miner

Variants studied for Episodic ataxia

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
0 0 114 113 45 272

Gene and significance breakdown #

Total genes and gene combinations: 4
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Gene or gene combination uncertain significance likely benign benign total
KCNA1 55 37 20 112
CACNB4 41 48 13 102
SLC1A3 17 28 12 57
CACNA1A 1 0 0 1

Submitter and significance breakdown #

Total submitters: 2
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Submitter uncertain significance likely benign benign total
Illumina Clinical Services Laboratory,Illumina 113 113 45 271
Institute of Human Genetics,University of Wuerzburg 1 0 0 1

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