ClinVar Miner

Variants studied for Fanconi anemia complementation group U

Included ClinVar conditions (2):
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 3 17 3 4 24

Gene and significance breakdown #

Total genes and gene combinations: 1
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Gene or gene combination likely pathogenic uncertain significance likely benign benign total
XRCC2 3 17 3 4 24

Submitter and significance breakdown #

Total submitters: 8
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Submitter likely pathogenic uncertain significance likely benign benign total
Mendelics 0 11 3 0 14
KCCC/NGS Laboratory, Kuwait Cancer Control Center 0 0 1 4 5
Fulgent Genetics, Fulgent Genetics 0 3 0 0 3
Baylor Genetics 0 2 0 0 2
Laboratorio de Genetica e Diagnostico Molecular, Hospital Israelita Albert Einstein 1 1 0 0 2
OMIM 0 1 0 0 1
Centogene AG - the Rare Disease Company 1 0 0 0 1
Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center 1 0 0 0 1

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