ClinVar Miner

Variants studied for Intellectual developmental disorder, autosomal recessive 69

Coded as:
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
11 0 7 0 1 19

Gene and significance breakdown #

Total genes and gene combinations: 1
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Gene or gene combination pathogenic uncertain significance benign total
ZBTB11 11 7 1 19

Submitter and significance breakdown #

Total submitters: 6
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Submitter pathogenic uncertain significance benign total
OMIM 9 0 0 9
Baylor Genetics 0 3 0 3
Revvity Omics, Revvity 0 3 0 3
Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre 0 2 0 2
Women's Health and Genetics/Laboratory Corporation of America, LabCorp 2 0 0 2
Genome-Nilou Lab 0 0 1 1

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