ClinVar Miner

Variants studied for Dilated Cardiomyopathy, Recessive

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 0 124 52 17 193

Gene and significance breakdown #

Total genes and gene combinations: 5
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Gene or gene combination uncertain significance likely benign benign total
PLEKHM2 61 24 17 102
FKTN 55 5 0 60
DNAAF3, TNNI3 0 16 0 16
TNNI3 8 4 0 12
TNNI3, TNNT1 0 3 0 3

Submitter and significance breakdown #

Total submitters: 2
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Submitter uncertain significance likely benign benign total
Invitae 61 24 17 102
Illumina Clinical Services Laboratory,Illumina 63 28 0 91

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