ClinVar Miner

Variants from Laboratory of Human Molecular Genetics, Department of Medical Research,Taipei Veterans General Hospital

Location: Taiwan — Primary collection method: research
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
2 2 1 0 0 5

Gene and significance breakdown #

Total genes and gene combinations: 3
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Gene or gene combination pathogenic likely pathogenic uncertain significance total
FZD4, PRSS23 2 0 0 2
RCBTB1 0 2 0 2
NDP 0 0 1 1

Condition and significance breakdown #

Total conditions: 2
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Condition pathogenic likely pathogenic uncertain significance total
Exudative retinopathy; Familial exudative vitreoretinopathy 2 1 1 4
Exudative retinopathy 0 1 0 1

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