ClinVar Miner

Variants from Exeter Molecular Genetics Laboratory

Location: United Kingdom  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
4 9 2 0 0 15

Gene and significance breakdown #

Total genes and gene combinations: 4
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Gene or gene combination pathogenic likely pathogenic uncertain significance total
PPP1R13L 0 5 2 7
HNF4A 4 2 0 6
ROR2 0 1 0 1
TRPV6 0 1 0 1

Condition and significance breakdown #

Total conditions: 4
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Condition pathogenic likely pathogenic uncertain significance total
Primary dilated cardiomyopathy 0 5 2 7
Maturity-onset diabetes of the young type 1 4 2 0 6
Autosomal recessive Robinow syndrome 0 1 0 1
Slender long bone; Hyperparathyroidism; Embryonic calcium dysregulation; Metaphyseal fractures 0 1 0 1

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