ClinVar Miner

Variants studied for Homocystinuria

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
47 17 3 0 1 67

Gene and significance breakdown #

Total genes and gene combinations: 1
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Gene or gene combination pathogenic likely pathogenic uncertain significance benign total
CBS 47 17 3 1 67

Submitter and significance breakdown #

Total submitters: 4
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Submitter pathogenic likely pathogenic uncertain significance benign total
Women's Health and Genetics/Laboratory Corporation of America, LabCorp 47 16 0 0 63
Illumina Laboratory Services, Illumina 0 0 3 1 4
Centogene AG - the Rare Disease Company 0 1 0 0 1
Hadassah Hebrew University Medical Center 1 0 0 0 1

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