ClinVar Miner

Variants with conflicting interpretations "uncertain significance" from Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center and "likely benign" from Women's Health and Genetics/Laboratory Corporation of America, LabCorp

Minimum review status of the submission from Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center: Collection method of the submission from Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center:
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_001148.6(ANK2):c.8324A>G (p.His2775Arg) rs534934297 0.00006

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