ClinVar Miner

Variants studied for Deficiency of hyaluronoglucosaminidase

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
40 2 112 191 15 345

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
HYAL1 40 2 112 191 15 345

Submitter and significance breakdown #

Total submitters: 6
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign total
Invitae 38 1 83 189 7 318
Illumina Laboratory Services, Illumina 0 0 27 2 12 41
Natera, Inc. 0 0 13 4 7 24
OMIM 3 0 0 0 0 3
Women's Health and Genetics/Laboratory Corporation of America, LabCorp 0 1 0 0 0 1
Genome-Nilou Lab 0 0 0 0 1 1

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