ClinVar Miner

Variants studied for dilated cardiomyopathy 1FF

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
5 2 0 0 0 6

Gene and significance breakdown #

Total genes and gene combinations: 2
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Gene or gene combination pathogenic likely pathogenic total
TNNI3 4 2 5
KLF5 1 0 1

Submitter and significance breakdown #

Total submitters: 6
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Submitter pathogenic likely pathogenic total
OMIM 2 0 2
Fulgent Genetics,Fulgent Genetics 2 0 2
UCLA Clinical Genomics Center, UCLA 0 1 1
Division of Human Genetics,Children's Hospital of Philadelphia 0 1 1
Cardiovascular Research Laboratory,Shanghai Chest Hospital, Shanghai Jiao Tong University 1 0 1
Heart Center,Academic Medical Center Amsterdam 0 1 1

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