ClinVar Miner

Variants from Clinical Genomics Laboratory, Laboratory for Precision Diagnostics, University of Washington with conflicting interpretations

Location: United States  Primary collection method: clinical testing
Minimum review status of the submission from Clinical Genomics Laboratory, Laboratory for Precision Diagnostics, University of Washington: Collection method of the submission from Clinical Genomics Laboratory, Laboratory for Precision Diagnostics, University of Washington:
Minimum review status of the other submission: Collection method of the other submission:
Minimum conflict level:
ClinVar version:

If a variant has more than two submissions, it may have multiple conflicts and therefore be counted in more than one conflict column. If this is the case, the "Variants with any kind of conflict" cell will be less than the sum of the conflicted variants cells to its left.

Variants with only 1 submission per condition Variants with at least 2 submissions on the same condition and no conflicts Variants with a synonymous conflict
(e.g. benign vs non-pathogenic)
Variants with a confidence conflict
(e.g. benign vs likely benign)
Variants with a benign or likely benign vs uncertain conflict Variants with a category conflict
(e.g. benign vs affects)
Variants with a clinically significant conflict
(e.g. benign vs pathogenic)
Variants with any conflict
358 4 0 0 0 0 5 5

Significance breakdown #

In the table below, cells that correspond to a term paired with itself represent synonymous conflicts, i.e. variants that have been annotated with different terms that map to the same standard term. To compare the terms that were actually submitted, check the box in the filters section at the top of this page.

All submitters
Clinical Genomics Laboratory, Laboratory for Precision Diagnostics, University of Washington likely benign benign
pathogenic 2 2
likely pathogenic 1 0

Submitter to submitter summary #

Total submitters: 1
Download table as spreadsheet
Submitter Variants with only 1 submission per condition Variants with at least 2 submissions on the same condition and no conflicts Variants with a synonymous conflict
(e.g. benign vs non-pathogenic)
Variants with a confidence conflict
(e.g. benign vs likely benign)
Variants with a benign or likely benign vs uncertain conflict Variants with a category conflict
(e.g. benign vs affects)
Variants with a clinically significant conflict
(e.g. benign vs pathogenic)
Variants with any conflict
Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory, Cincinnati Children's Hospital Medical Center 0 4 0 0 0 0 5 5

All variants with conflicting interpretations #

Total variants: 5
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HGVS dbSNP gnomAD frequency
GRCh37/hg19 15q11.2(chr15:22750305-23109890)x1
GRCh37/hg19 15q11.2(chr15:22750305-23226254)x3
GRCh37/hg19 15q13.3(chr15:32019919-32514341)x3
GRCh37/hg19 22q11.21(chr22:20733495-21463730)x1
GRCh37/hg19 22q11.21(chr22:21062168-21463730)x1

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