ClinVar Miner

Variants studied for Fanconi anemia, complementation group Q

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
4 1 16 0 5 26

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
ERCC4 4 1 16 5 26

Submitter and significance breakdown #

Total submitters: 6
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Submitter pathogenic likely pathogenic uncertain significance benign total
Baylor Genetics 0 0 15 0 15
Nilou-Genome Lab 0 0 0 5 5
OMIM 4 0 0 0 4
Leiden Open Variation Database 3 0 0 0 3
Centre for Mendelian Genomics,University Medical Centre Ljubljana 0 0 1 0 1
St. Jude Clinical Genomics Lab, St. Jude Children's Research Hospital 0 1 0 0 1

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