ClinVar Miner

Variants studied for Charcot-Marie-Tooth disease, axonal, with vocal cord paresis, autosomal recessive

Included ClinVar conditions (3):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:

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 not provided total
13 14 64 8 17 3 115

Gene and significance breakdown #

Total genes and gene combinations: 2
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Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign benign not provided total
GDAP1 10 11 63 8 16 3 107
GDAP1, LOC130000622 3 3 1 0 1 0 8

Submitter and significance breakdown #

Total submitters: 12
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign not provided total
Illumina Laboratory Services, Illumina 0 0 60 8 15 0 83
Fulgent Genetics, Fulgent Genetics 9 12 3 0 0 0 24
Kariminejad - Najmabadi Pathology & Genetics Center 2 2 1 0 0 0 5
3billion 0 1 1 0 0 0 2
Genome-Nilou Lab 0 0 0 0 2 0 2
GenomeConnect - Invitae Patient Insights Network 0 0 0 0 0 2 2
First Genomix Gene Laboratory, Genetic Diagnostics Department 1 0 0 0 0 0 1
GeneReviews 0 0 0 0 0 1 1
Juno Genomics, Hangzhou Juno Genomics, Inc 0 1 0 0 0 0 1
MGZ Medical Genetics Center 1 0 0 0 0 0 1
OMIM 1 0 0 0 0 0 1
UCLA Clinical Genomics Center, UCLA 1 0 0 0 0 0 1

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