ClinVar Miner

Variants from Versiti Diagnostic Laboratories, Versiti, Inc

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
8 0 0 1 1 10

Gene and significance breakdown #

Total genes and gene combinations: 2
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Gene or gene combination pathogenic likely benign benign total
VWF 8 0 1 9
F8 0 1 0 1

Condition and significance breakdown #

Total conditions: 6
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Condition pathogenic likely benign benign total
Von Willebrand disease type 2B 3 0 0 3
Von Willebrand disease type 2A 2 0 0 2
von Willebrand disease type 2M 1 0 1 2
Hereditary factor VIII deficiency disease 0 1 0 1
Von Willebrand disease type 2A; von Willebrand disease type 1; von Willebrand disease type 2M 1 0 0 1
von Willebrand disease type 2N 1 0 0 1

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