ClinVar Miner

Variants from Urologic Oncology Branch, National Institutes of Health

Location: United States  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 total
50 0 0 0 0 50

Gene and significance breakdown #

Total genes and gene combinations: 5
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Gene or gene combination pathogenic total
LOC107303340, VHL 30 30
VHL 10 10
IRAK2, VHL 4 4
LOC107303339, LOC107303340, VHL 4 4
BRK1, VHL 2 2

Condition and significance breakdown #

Total conditions: 1
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Condition pathogenic total
Von Hippel-Lindau syndrome 50 50

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