ClinVar Miner

Variants studied for Larsen-like syndrome, B3GAT3 type

Included ClinVar conditions (1):
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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
2 1 3 0 3 9

Gene and significance breakdown #

Total genes and gene combinations: 3
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Gene or gene combination pathogenic likely pathogenic uncertain significance benign total
B3GAT3 2 0 2 3 7
B4GALT7 0 1 0 0 1
COL11A2 0 0 1 0 1

Submitter and significance breakdown #

Total submitters: 7
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Submitter pathogenic likely pathogenic uncertain significance benign total
Invitae 1 0 1 2 4
Developmental Genetics Unit,King Faisal Specialist Hospital & Research Centre 0 1 1 0 2
Baylor Miraca Genetics Laboratories, 1 0 0 0 1
Genome Diagnostics Laboratory,University Medical Center Utrecht 0 0 0 1 1
Mayo Clinic Genetic Testing Laboratories,Mayo Clinic 0 0 1 0 1
Fulgent Genetics 0 0 1 0 1
DNA and Cytogenetics Diagnostics Unit,Erasmus Medical Center 0 0 0 1 1

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