ClinVar Miner

Variants studied for bile duct adenocarcinoma

Included ClinVar conditions (3):
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 other total
1 0 4 0 0 11 16

Gene and significance breakdown #

Total genes and gene combinations: 13
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Gene or gene combination pathogenic uncertain significance other total
APC 0 4 0 4
​intergenic 1 0 0 1
CXCL8 0 0 1 1
CXCR1 0 0 1 1
EGF 0 0 1 1
EGFR 0 0 1 1
HIF1A 0 0 1 1
IL10, IL19 0 0 1 1
IL1B 0 0 1 1
IL6, LOC126859963 0 0 1 1
PACERR, PTGS2 0 0 1 1
POLR1C, VEGFA 0 0 1 1
PTGS2 0 0 1 1

Submitter and significance breakdown #

Total submitters: 3
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Submitter pathogenic uncertain significance other total
Department of Surgery, Campus Charité Mitte | Campus Virchow-klinikum, Charite-Universitaetsmedizin Berlin 0 0 11 11
3DMed Clinical Laboratory Inc 0 4 0 4
OSU Cancer Genomics Laboratory, Ohio State University Medical Center 1 0 0 1

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