ClinVar Miner

Variants with conflicting interpretations "likely benign" from The Genetics Institute, Rambam Health Care Campus and "likely pathogenic" from any submitter

Minimum review status of the submission from The Genetics Institute, Rambam Health Care Campus: Collection method of the submission from The Genetics Institute, Rambam Health Care Campus:
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_032590.5(KDM2B):c.3050G>A (p.Arg1017His) rs782304760 0.00003

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