ClinVar Miner

Variants studied for Heimler syndrome 2

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
11 2 6 0 10 29

Gene and significance breakdown #

Total genes and gene combinations: 1
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Gene or gene combination pathogenic likely pathogenic uncertain significance benign total
PEX6 11 2 6 10 29

Submitter and significance breakdown #

Total submitters: 7
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Submitter pathogenic likely pathogenic uncertain significance benign total
Nilou-Genome Lab 0 0 1 10 11
Leeds Amelogenesis Imperfecta Research Group, University of Leeds 7 0 0 0 7
OMIM 5 0 0 0 5
Baylor Genetics 0 0 4 0 4
Clinical Genetics laboratory, University of Goettingen 0 1 0 0 1
Hadassah Hebrew University Medical Center 0 1 0 0 1
Institute of Human Genetics, University of Leipzig Medical Center 0 0 1 0 1

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