ClinVar Miner

Variants studied for Donohue syndrome

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
18 0 57 67 35 177

Gene and significance breakdown #

Total genes and gene combinations: 1
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Gene or gene combination pathogenic uncertain significance likely benign benign total
INSR 18 57 67 35 177

Submitter and significance breakdown #

Total submitters: 6
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Submitter pathogenic uncertain significance likely benign benign total
Illumina Clinical Services Laboratory,Illumina 0 53 67 35 155
OMIM 15 0 0 0 15
Fulgent Genetics,Fulgent Genetics 0 4 0 0 4
GeneReviews 2 0 0 0 2
Genetic Services Laboratory, University of Chicago 1 0 0 0 1
Medical Research Institute,Tokyo Medical and Dental University 1 0 0 0 1

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