ClinVar Miner

Variants with conflicting interpretations "likely pathogenic" from Institute of Neurogenomics,Technical University of Munich and "uncertain significance" from any submitter

Minimum review status of the submission from Institute of Neurogenomics,Technical University of Munich: Collection method of the submission from Institute of Neurogenomics,Technical University of Munich:
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
NM_001744.6(CAMK4):c.981+1G>A rs1561515242

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