ClinVar Miner

Variants studied for Grn-related frontotemporal lobar degeneration with Tdp43 inclusions

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
31 0 29 17 15 87

Gene and significance breakdown #

Total genes and gene combinations: 1
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Gene or gene combination pathogenic uncertain significance likely benign benign total
GRN 31 29 17 15 87

Submitter and significance breakdown #

Total submitters: 7
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Submitter pathogenic uncertain significance likely benign benign total
Illumina Clinical Services Laboratory,Illumina 0 29 17 7 53
OMIM 15 0 0 0 15
Institute of Human Genetics,Klinikum rechts der Isar 12 0 0 0 12
Athena Diagnostics Inc 0 0 0 9 9
Mendelics 2 0 0 1 3
GeneReviews 3 0 0 0 3
Center of Genomic medicine, Geneva,University Hospital of Geneva 2 0 0 0 2

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