ClinVar Miner

Variants with conflicting interpretations "likely pathogenic" from Molecular Diagnostics Laboratory, M Health Fairview: University of Minnesota and "likely pathogenic" from any submitter

Minimum review status of the submission from Molecular Diagnostics Laboratory, M Health Fairview: University of Minnesota: Collection method of the submission from Molecular Diagnostics Laboratory, M Health Fairview: University of Minnesota:
Minimum review status of the other submission: Collection method of the other submission:
ClinVar version:
Total variants with conflicting interpretations: 1
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HGVS dbSNP gnomAD frequency
NM_152564.5(VPS13B):c.11832dup (p.Ser3945fs) rs180177374

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