ClinVar Miner

Variants from Neuromuscular Diagnostic Laboratory, American University of Beirut Medical Center

Location: Lebanon  Primary collection method: research
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
5 0 0 0 0 5

Gene and significance breakdown #

Total genes and gene combinations: 2
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Gene or gene combination pathogenic total
DMD 3 3
CAPN3 2 2

Condition and significance breakdown #

Total conditions: 2
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Condition pathogenic total
Duchenne muscular dystrophy 3 3
Autosomal recessive limb-girdle muscular dystrophy type 2A 2 2

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