ClinVar Miner

Variants studied for Fanconi anemia, complementation group D1

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
22 1 111 62 28 221

Gene and significance breakdown #

Total genes and gene combinations: 2
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Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign benign total
BRCA2 22 1 108 61 27 216
BRCA2, LOC106721785 0 0 3 1 1 5

Submitter and significance breakdown #

Total submitters: 6
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign total
Illumina Clinical Services Laboratory,Illumina 0 0 111 62 27 200
OMIM 15 0 0 0 0 15
Biochemical Molecular Genetic Laboratory,King Abdulaziz Medical City 2 1 0 0 1 4
Medical Genetics Institute,Shaare Zedek Medical Center 2 0 0 0 0 2
Daryl Scott Lab,Baylor College of Medicine 2 0 0 0 0 2
Molecular Diagnostics Laboratory, M Health Fairview: University of Minnesota 1 0 0 0 0 1

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