ClinVar Miner

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

Location: India  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
14 6 25 1 0 46

Gene and significance breakdown #

Total genes and gene combinations: 4
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Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign total
MYH7 11 5 15 1 32
TNNT2 2 0 4 0 6
LOC126861898, MYH7 1 0 3 0 4
TPM1 0 1 3 0 4

Condition and significance breakdown #

Total conditions: 5
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Condition pathogenic likely pathogenic uncertain significance likely benign total
Familial cardiomyopathy 12 5 18 1 36
Dilated cardiomyopathy 1DD 1 0 4 0 5
Cardiomyopathy 0 1 2 0 3
Primary familial hypertrophic cardiomyopathy 1 0 0 0 1
not provided 0 0 1 0 1

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