ClinVar Miner

Variants from Research Unit of Biomedicine, University of Oulu

Location: Finland  Primary collection method: clinical testing
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 likely pathogenic, low penetrance total
0 0 0 0 0 1 1

Gene and significance breakdown #

Total genes and gene combinations: 1
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Gene or gene combination likely pathogenic, low penetrance total
KLF2 1 1

Condition and significance breakdown #

Total conditions: 1
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Condition likely pathogenic, low penetrance total
Inherited Immunodeficiency Diseases 1 1

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