ClinVar Miner

Variants studied for Primary hyperoxaluria, type III

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
32 15 27 0 0 64

Gene and significance breakdown #

Total genes and gene combinations: 1
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Gene or gene combination pathogenic likely pathogenic uncertain significance total
HOGA1 32 15 27 64

Submitter and significance breakdown #

Total submitters: 9
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Submitter pathogenic likely pathogenic uncertain significance total
Clinical Biochemistry Laboratory,Health Services Laboratory 29 0 11 40
Counsyl 3 12 15 30
OMIM 8 0 0 8
Illumina Clinical Services Laboratory,Illumina 3 2 1 6
Bioscientia Institut fuer Medizinische Diagnostik GmbH,Sonic Healthcare 1 1 1 3
Laboratory for Molecular Medicine, Partners HealthCare Personalized Medicine 2 0 0 2
GeneReviews 2 0 0 2
Fulgent Genetics,Fulgent Genetics 2 0 0 2
Reproductive Health Research and Development,BGI Genomics 1 0 0 1

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