ClinVar Miner

Variants studied for Lymphangiomyomatosis; Tuberous sclerosis 1; Isolated focal cortical dysplasia type II

Coded as:
Minimum submission review status: Collection method:
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Gene type:
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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
9 2 43 40 3 97

Gene and significance breakdown #

Total genes and gene combinations: 1
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Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign benign total
TSC1 9 2 43 40 3 97

Submitter and significance breakdown #

Total submitters: 4
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign total
Fulgent Genetics, Fulgent Genetics 6 1 42 38 3 90
Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago 2 1 1 1 0 5
Juno Genomics, Hangzhou Juno Genomics, Inc 2 0 0 0 0 2
3billion 0 0 0 2 0 2

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