ClinVar Miner

Variants in gene C11orf65

See also:
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
0 0 3 0 2 5

Condition and significance breakdown #

Total conditions: 2
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Condition uncertain significance benign total
not provided 1 2 3
Inborn genetic diseases 2 0 2

Submitter and significance breakdown #

Total submitters: 3
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Submitter uncertain significance benign total
Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory, Cincinnati Children's Hospital Medical Center 0 2 2
Ambry Genetics 2 0 2
Quest Diagnostics Nichols Institute San Juan Capistrano 1 0 1

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