ClinVar Miner

Variants with conflicting interpretations "uncertain significance" from Michigan Medical Genetics Laboratories,University of Michigan and "likely benign" from Genome Diagnostics Laboratory,University Medical Center Utrecht

Minimum review status of the submission from Michigan Medical Genetics Laboratories,University of Michigan: Collection method of the submission from Michigan Medical Genetics Laboratories,University of Michigan:
Minimum review status of the other submission: Collection method of the other submission:
ClinVar version:
Total variants with conflicting interpretations: 3
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HGVS dbSNP
NM_000059.3(BRCA2):c.476-9dup rs276174849
NM_000059.3(BRCA2):c.67+4T>C rs373546450
NM_000059.4(BRCA2):c.9501+3A>T rs61757642

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