ClinVar Miner

Variants with conflicting interpretations "pathogenic" from Laboratory of Genetics and Genomics,Institute for Developing Science and Health Initiatives Foundation and "likely pathogenic" from any submitter

Minimum review status of the submission from Laboratory of Genetics and Genomics,Institute for Developing Science and Health Initiatives Foundation: Collection method of the submission from Laboratory of Genetics and Genomics,Institute for Developing Science and Health Initiatives Foundation:
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_002225.5(IVD):c.960G>T (p.Gln320His) rs367814475

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