ClinVar Miner

Variants from Genetics Laboratories, Oxford Radcliffe Hospitals NHS Trust

Location: United Kingdom — Primary collection method: not provided
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 2 19 5 26

Gene and significance breakdown #

Total genes and gene combinations: 1
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Gene or gene combination uncertain significance likely benign benign total
TCOF1 2 19 5 26

Condition and significance breakdown #

Total conditions: 1
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Condition uncertain significance likely benign benign total
Treacher Collins syndrome 1 2 19 5 26

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