ClinVar Miner

Variants from RBC Disorders, Laboratory of Genetics and Genomics, Cincinnati Children's Hospital Medical Center

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
2 1 0 0 0 3

Gene and significance breakdown #

Total genes and gene combinations: 2
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Gene or gene combination pathogenic likely pathogenic total
VPS4A 2 0 2
LOC126862382, VPS4A 0 1 1

Condition and significance breakdown #

Total conditions: 1
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Condition pathogenic likely pathogenic total
Syndromic congenital hemolytic and dyserythropoietic anemia 2 1 3

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