ClinVar Miner

Variants from Evolutionary and Medical Genetics Laboratory, Center for Cellular and Molecular Biology

Location: India  Primary collection method: case-control
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 1 0 0 0 1

Gene and significance breakdown #

Total genes and gene combinations: 1
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Gene or gene combination likely pathogenic total
TCAP 1 1

Condition and significance breakdown #

Total conditions: 1
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Condition likely pathogenic total
Autosomal recessive limb-girdle muscular dystrophy type 2G 1 1

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