ClinVar Miner

Variants studied for Corticosterone methyloxidase type 2 deficiency

Coded as:
Minimum submission review status: Collection method:
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Gene type:
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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 not provided total
7 1 56 12 38 1 114

Gene and significance breakdown #

Total genes and gene combinations: 2
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Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign benign not provided total
CYP11B2, LOC106799834 7 1 56 11 38 1 113
CYP11B2, LOC106799834, LOC110673971 0 0 0 1 0 0 1

Submitter and significance breakdown #

Total submitters: 7
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign not provided total
Illumina Laboratory Services, Illumina 0 0 56 12 24 0 92
Genome-Nilou Lab 0 0 0 0 21 0 21
3billion 3 1 1 0 0 0 5
OMIM 4 0 0 0 0 0 4
Clinical Biochemistry Laboratory, Health Services Laboratory 2 0 0 0 0 0 2
Mendelics 0 0 0 0 1 0 1
GenomeConnect, ClinGen 0 0 0 0 0 1 1

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