ClinVar Miner

Variants in gene combination B3GALT2, CDC73

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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
0 0 2 2 1 5

Condition and significance breakdown #

Total conditions: 4
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Condition uncertain significance likely benign benign total
See cases 1 1 0 2
Hyperparathyroidism 2 0 1 0 1
Parathyroid carcinoma 1 0 0 1
not provided 0 0 1 1

Submitter and significance breakdown #

Total submitters: 5
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Submitter uncertain significance likely benign benign total
Invitae 1 0 0 1
ISCA site 1 1 0 0 1
ISCA site 6 0 1 0 1
CSER_CC_NCGL; University of Washington Medical Center 0 1 0 1
Laboratory of Genetics and Genomics,Cincinnati Children's Hospital Medical Center 0 0 1 1

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