ClinVar Miner

Variants with conflicting interpretations "likely pathogenic" from Laboratory of Molecular Genetics, CHU Rennes and "uncertain significance" from any submitter

Minimum review status of the submission from Laboratory of Molecular Genetics, CHU Rennes: Collection method of the submission from Laboratory of Molecular Genetics, CHU Rennes:
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_000834.5(GRIN2B):c.1672G>A (p.Val558Ile) rs1057519004

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