ClinVar Miner

Variants studied for Epilepsy, idiopathic generalized 9

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 risk factor total
1 0 1 0 0 1 3

Gene and significance breakdown #

Total genes and gene combinations: 1
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Gene or gene combination pathogenic uncertain significance risk factor total
CACNB4 1 1 1 3

Submitter and significance breakdown #

Total submitters: 3
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Submitter pathogenic uncertain significance risk factor total
OMIM 0 0 1 1
Baylor Miraca Genetics Laboratories, 1 0 0 1
Mayo Clinic Genetic Testing Laboratories,Mayo Clinic 0 1 0 1

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