ClinVar Miner

Variants from U4M - Lille University & CHRU Lille, Université de Lille - CHRU de Lille

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
299 43 0 4 0 346

Gene and significance breakdown #

Total genes and gene combinations: 2
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Gene or gene combination pathogenic likely pathogenic likely benign total
LDLR 297 43 4 344
LDLR, MIR6886 2 0 0 2

Condition and significance breakdown #

Total conditions: 1
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Condition pathogenic likely pathogenic likely benign total
Familial hypercholesterolemia 1 299 43 4 346

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