ClinVar Miner

Variants studied for colorectal cancer, susceptibility to, 1

Included ClinVar conditions (1):
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 risk factor total
0 0 114 1 0 3 118

Gene and significance breakdown #

Total genes and gene combinations: 3
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Gene or gene combination uncertain significance likely benign risk factor total
GALNT12 108 1 3 112
GALNT12, LOC130002222 5 0 0 5
ATM 1 0 0 1

Submitter and significance breakdown #

Total submitters: 4
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Submitter uncertain significance likely benign risk factor total
Baylor Genetics 107 0 0 107
Fulgent Genetics, Fulgent Genetics 7 1 0 8
OMIM 0 0 3 3
KCCC/NGS Laboratory, Kuwait Cancer Control Center 1 0 0 1

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