ClinVar Miner

Variants studied for Atrial fibrillation, familial, 7

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
6 0 152 82 21 233

Gene and significance breakdown #

Total genes and gene combinations: 1
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Gene or gene combination pathogenic uncertain significance likely benign benign total
KCNA5 6 152 82 21 233

Submitter and significance breakdown #

Total submitters: 9
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Submitter pathogenic uncertain significance likely benign benign total
Invitae 0 112 73 17 202
Illumina Clinical Services Laboratory,Illumina 0 36 8 5 49
ARUP Laboratories, Molecular Genetics and Genomics,ARUP Laboratories 0 2 2 4 8
OMIM 6 0 0 0 6
Centre for Mendelian Genomics,University Medical Centre Ljubljana 0 4 0 0 4
Fulgent Genetics,Fulgent Genetics 0 2 0 0 2
Clinical Genetics laboratory, University of Goettingen 0 1 0 0 1
Mendelics 0 1 0 0 1
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen 0 0 0 1 1

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