ClinVar Miner

Variants with conflicting interpretations "likely benign" from Center for Advanced Laboratory Medicine, UC San Diego Health, University of California San Diego and "benign" from ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

Minimum review status of the submission from Center for Advanced Laboratory Medicine, UC San Diego Health, University of California San Diego: Collection method of the submission from Center for Advanced Laboratory Medicine, UC San Diego Health, University of California San Diego:
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_017636.4(TRPM4):c.3611C>T (p.Pro1204Leu) rs150391806 0.00310

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