ClinVar Miner

Variants with conflicting interpretations "uncertain significance" from Molecular Genetics Laboratory, Institute for Ophthalmic Research and "pathogenic" from any submitter

Minimum review status of the submission from Molecular Genetics Laboratory, Institute for Ophthalmic Research: Collection method of the submission from Molecular Genetics Laboratory, Institute for Ophthalmic Research:
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_001377295.2(GNAT2):c.461+24G>A rs397515384

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