ClinVar Miner

Variants studied for atrial fibrillation, familial, 11

Included ClinVar conditions (3):
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
7 0 177 69 5 252

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
GJA5 5 133 54 4 190
GJA5, LOC122128420 2 44 15 1 62

Submitter and significance breakdown #

Total submitters: 5
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Submitter pathogenic uncertain significance likely benign benign total
Invitae 0 154 68 5 227
Illumina Laboratory Services, Illumina 0 26 1 0 27
OMIM 6 0 0 0 6
Baylor Genetics 1 0 0 0 1
Fulgent Genetics, Fulgent Genetics 0 1 0 0 1

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