ClinVar Miner

Variants from Medical Genetics and Mitochondrial Research group, Latvian Biomedical Research and Study center

Location: Latvia  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
3 1 0 0 0 4

Gene and significance breakdown #

Total genes and gene combinations: 4
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Gene or gene combination pathogenic likely pathogenic total
CAPN3 0 1 1
HPDL 1 0 1
LAMP2 1 0 1
MYBPC1 1 0 1

Condition and significance breakdown #

Total conditions: 4
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Condition pathogenic likely pathogenic total
Autosomal recessive limb-girdle muscular dystrophy type 2A 0 1 1
Danon disease 1 0 1
Neurodevelopmental disorder with progressive spasticity and brain white matter abnormalities 1 0 1
not provided 1 0 1

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