ClinVar Miner

Variants studied for FANCM Fanconi-like genomic instability disorder

Included ClinVar conditions (1):
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 total
0 2 0 0 0 2

Gene and significance breakdown #

Total genes and gene combinations: 1
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Gene or gene combination likely pathogenic total
FANCM 2 2

Submitter and significance breakdown #

Total submitters: 2
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Submitter likely pathogenic total
Department of Pathology and Laboratory Medicine, Sinai Health System 1 1
Zero Childhood Cancer Program, Children's Cancer Institute 1 1

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