ClinVar Miner

Variants with conflicting interpretations "likely benign" from EGL Genetic Diagnostics, Eurofins Clinical Diagnostics and "pathogenic" from Institute of Medical Genetics and Applied Genomics, University Hospital Tübingen

Minimum review status of the submission from EGL Genetic Diagnostics, Eurofins Clinical Diagnostics: Collection method of the submission from EGL Genetic Diagnostics, Eurofins Clinical Diagnostics:
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_201253.3(CRB1):c.498_506del (p.Ile167_Gly169del) rs398124615

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