ClinVar Miner

Variants studied for Osteogenesis Imperfecta, Dominant

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
0 0 101 41 10 151

Gene and significance breakdown #

Total genes and gene combinations: 2
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Gene or gene combination uncertain significance likely benign benign total
COL1A1 70 20 0 89
COL1A2 31 21 10 62

Submitter and significance breakdown #

Total submitters: 1
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Submitter uncertain significance likely benign benign total
Illumina Clinical Services Laboratory,Illumina 101 41 10 151

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