ClinVar Miner

Variants with conflicting interpretations "likely pathogenic" from Institute for Genomic Medicine, Nationwide Children's Hospital and "uncertain significance" from Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center

Minimum review status of the submission from Institute for Genomic Medicine, Nationwide Children's Hospital: Collection method of the submission from Institute for Genomic Medicine, Nationwide Children's Hospital:
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_000053.4(ATP7B):c.3045G>A (p.Leu1015=) rs1801248 0.02598

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