ClinVar Miner

Variants from Constitutional Genetics Lab, Leon Berard Cancer Center

Location: France  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
105 13 22 0 0 140

Gene and significance breakdown #

Total genes and gene combinations: 4
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Gene or gene combination pathogenic likely pathogenic uncertain significance total
MLH1 46 7 5 58
MSH2 38 2 3 43
MSH6 19 4 9 32
PMS2 2 0 5 7

Condition and significance breakdown #

Total conditions: 1
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Condition pathogenic likely pathogenic uncertain significance total
Lynch-like syndrome 105 13 22 140

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