ClinVar Miner

Variants studied for Glycogen storage disease due to lactate dehydrogenase M-subunit deficiency

Coded as:
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
5 2 87 54 13 151

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 total
LDHA 5 2 86 54 13 150
GTF2H1, HPS5, LDHA 0 0 1 0 0 1

Submitter and significance breakdown #

Total submitters: 9
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign total
Labcorp Genetics (formerly Invitae), Labcorp 3 2 48 49 9 111
Illumina Laboratory Services, Illumina 0 0 37 5 9 51
Fulgent Genetics, Fulgent Genetics 0 0 2 6 0 8
Genome-Nilou Lab 0 0 0 0 3 3
OMIM 1 0 1 0 0 2
Revvity Omics, Revvity 0 0 2 0 0 2
Baylor Genetics 0 0 1 0 0 1
Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center 0 0 1 0 0 1
Institute of Human Genetics Munich, Klinikum Rechts Der Isar, TU München 1 0 0 0 0 1

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