ClinVar Miner

Variants from Leeds Vision Research Group,University of Leeds

Location: United Kingdom — Primary collection method: reference population
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
10 0 0 0 0 10

Gene and significance breakdown #

Total genes and gene combinations: 2
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Gene or gene combination pathogenic total
DRAM2 7 7
CTNNB1 3 3

Condition and significance breakdown #

Total conditions: 2
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Condition pathogenic total
Retinal dystrophy 7 7
Exudative vitreoretinopathy 1 3 3

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