ClinVar Miner

Variants from Fundacion Hipercolesterolemia Familiar

Location: Spain  Primary collection method: research
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
129 77 113 5 5 329

Gene and significance breakdown #

Total genes and gene combinations: 5
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Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign benign total
LDLR 125 77 103 4 4 313
APOB 1 0 8 1 0 10
LDLR, MIR6886 3 0 1 0 0 4
LDLR, LOC126862855, LOC126862856 0 0 1 0 0 1
PCSK9 0 0 0 0 1 1

Condition and significance breakdown #

Total conditions: 1
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Condition pathogenic likely pathogenic uncertain significance likely benign benign total
Hypercholesterolemia, familial, 1 129 77 113 5 5 329

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