Variants with conflicting interpretations "pathogenic" from RettBASE and "risk factor" from OMIM

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)
		ClinVar version:

Total variants with conflicting interpretations: 2

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HGVS	dbSNP	gnomAD frequency
NM_001110792.2(MECP2):c.1193_1233del (p.Leu398fs)	rs267608327
NM_001110792.2(MECP2):c.916C>T (p.Arg306Ter)	rs61751362

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