ClinVar Miner

Variants studied for Arrhythmogenic right ventricular dysplasia, familial, 13

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
2 0 145 16 30 192

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
CTNNA3 2 144 16 30 191
CTNNA3, LOC101928961, LRRTM3 0 1 0 0 1

Submitter and significance breakdown #

Total submitters: 6
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Submitter pathogenic uncertain significance likely benign benign total
Invitae 0 142 16 30 188
OMIM 2 0 0 0 2
Fulgent Genetics,Fulgent Genetics 0 2 0 0 2
Mendelics 0 1 0 0 1
Soonchunhyang University Bucheon Hospital,Soonchunhyang University Medical Center 0 1 0 0 1
Phosphorus, Inc. 0 1 0 0 1

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