ClinVar Miner

Variants studied for Knobloch syndrome 2

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:

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 2 2 0 0 4

Gene and significance breakdown #

Total genes and gene combinations: 1
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Gene or gene combination likely pathogenic uncertain significance total
PAK2 2 2 4

Submitter and significance breakdown #

Total submitters: 4
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Submitter likely pathogenic uncertain significance total
Advanced Precision Medicine Laboratory, The Jackson Laboratory for Genomic Medicine 1 0 1
Fulgent Genetics, Fulgent Genetics 0 1 1
Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre 0 1 1
Laboratoire de Génétique Moléculaire, CHU Bordeaux 1 0 1

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