ClinVar Miner

Variants with conflicting interpretations "pathogenic" from RettBASE and "likely pathogenic" from Centre de Biologie Pathologie Génétique, Centre Hospitalier Universitaire de Lille

Minimum review status of the submission from RettBASE:		Collection method of the submission from RettBASE:
Minimum review status of the other submission:		Collection method of the other submission:
Show significances as they were submitted (without aggregation into standard terms)
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Total variants with conflicting interpretations: 1

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HGVS	dbSNP	gnomAD frequency
NM_001110792.2(MECP2):c.710C>G (p.Pro237Arg)	rs61749715

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