ClinVar Miner

Variants studied for corneal dystrophy, Fuchs endothelial, 3

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
3 0 2 0 0 5

Gene and significance breakdown #

Total genes and gene combinations: 1
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Gene or gene combination pathogenic uncertain significance total
TCF4 3 2 5

Submitter and significance breakdown #

Total submitters: 5
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Submitter pathogenic uncertain significance total
OMIM 1 0 1
Mayo Clinic Genetic Testing Laboratories,Mayo Clinic 1 0 1
Genomic Research Center,Shahid Beheshti University of Medical Sciences 0 1 1
Geisinger Autism and Developmental Medicine Institute,Geisinger Health System 0 1 1
Laboratoire de Cytogenetique,Hospices Civils de Lyon 1 0 1

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