ClinVar Miner

Variants studied for dilated cardiomyopathy 1II

Included ClinVar conditions (2):
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
12 3 127 66 7 211

Gene and significance breakdown #

Total genes and gene combinations: 2
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Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign benign total
CRYAB 12 3 126 66 7 210
C11orf52, CRYAB, DIXDC1, DLAT, HSPB2, NKAPD1, PIH1D2, SDHD, TIMM8B 0 0 1 0 0 1

Submitter and significance breakdown #

Total submitters: 5
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign total
Invitae 10 2 126 65 7 210
Fulgent Genetics, Fulgent Genetics 1 0 13 1 0 15
OMIM 2 0 0 0 0 2
Victorian Clinical Genetics Services, Murdoch Childrens Research Institute 0 1 0 0 0 1
Zotz-Klimas Genetics Lab, MVZ Zotz Klimas 0 0 1 0 0 1

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