ClinVar Miner

Variants from Familial Cancer Clinic, Veneto Institute of Oncology

Location: Italy  Primary collection method: not provided
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
0 19 0 0 0 19

Gene and significance breakdown #

Total genes and gene combinations: 2
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Gene or gene combination likely pathogenic total
TMEM127 15 15
LOC129934333, TMEM127 4 4

Condition and significance breakdown #

Total conditions: 1
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Condition likely pathogenic total
Pheochromocytoma 19 19

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