ClinVar Miner

Variants studied for Fanconi anemia, complementation group G

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 1 48 6 7 107

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
FANCG 46 1 47 4 4 101
FANCG, VCP 1 0 1 2 3 6

Submitter and significance breakdown #

Total submitters: 8
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign total
Illumina Clinical Services Laboratory,Illumina 0 0 37 6 7 50
Leiden Open Variation Database 41 1 7 0 0 49
OMIM 8 0 0 0 0 8
GeneReviews 5 0 0 0 0 5
Fulgent Genetics,Fulgent Genetics 1 0 3 0 0 4
Molecular Diagnostics Laboratory, M Health: University of Minnesota 4 0 0 0 0 4
Baylor Genetics 1 0 0 0 0 1
Genomic Research Center, Shahid Beheshti University of Medical Sciences 0 0 1 0 0 1

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