ClinVar Miner

Variants studied for AXIN2-related attenuated familial adenomatous polyposis

Included ClinVar conditions (2):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:

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 not provided total
5 5 0 0 0 1 11

Gene and significance breakdown #

Total genes and gene combinations: 1
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Gene or gene combination pathogenic likely pathogenic not provided total
AXIN2 5 5 1 11

Submitter and significance breakdown #

Total submitters: 2
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Submitter pathogenic likely pathogenic not provided total
Centre de Biologie Pathologie Génétique, Centre Hospitalier Universitaire de Lille 5 5 0 10
GenomeConnect, ClinGen 0 0 1 1

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