ClinVar Miner

Variants in gene GALNT12

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 0 310 140 22 3 446

Condition and significance breakdown #

Total conditions: 7
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Condition uncertain significance likely benign benign risk factor total
not provided 204 80 19 0 302
Hereditary cancer-predisposing syndrome 177 91 7 0 274
not specified 10 1 0 0 11
Colorectal cancer 1 7 0 0 3 10
Adenomatous polyposis coli, attenuated 0 0 1 0 1
Breast neoplasm 0 1 0 0 1
Colorectal cancer 1 0 0 0 1

Submitter and significance breakdown #

Total submitters: 9
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Submitter uncertain significance likely benign benign risk factor total
Invitae 207 80 19 0 305
Ambry Genetics 176 89 7 0 272
Fulgent Genetics,Fulgent Genetics 6 0 0 0 6
OMIM 0 0 0 3 3
University of Washington Department of Laboratory Medicine, University of Washington 1 2 0 0 3
CSER _CC_NCGL, University of Washington 1 0 0 0 1
Department of Pathology and Laboratory Medicine,Sinai Health System 0 1 0 0 1
Molecular Oncology Laboratory,Hospital Clínico San Carlos 0 0 1 0 1
ACT Genomics, 0 1 0 0 1

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