ClinVar Miner

Variants from Genetic Diagnostic Laboratory, University of Pennsylvania School of Medicine

Location: United States  Primary collection method: clinical testing
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:

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
368 31 43 15 1 458

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 total
RB1 368 30 42 15 1 456
RB1, RB1-DT 0 1 1 0 0 2

Condition and significance breakdown #

Total conditions: 1
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Condition pathogenic likely pathogenic uncertain significance likely benign benign total
Retinoblastoma 368 31 43 15 1 458

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