Variants with conflicting interpretations "pathogenic" from Genetics and Prenatal Diagnosis Center, The First Affiliated Hospital of Zhengzhou University and "likely pathogenic" from any submitter

Minimum review status of the submission from Genetics and Prenatal Diagnosis Center, The First Affiliated Hospital of Zhengzhou University:		Collection method of the submission from Genetics and Prenatal Diagnosis Center, The First Affiliated Hospital of Zhengzhou University:
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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001110792.2(MECP2):c.953G>T (p.Arg318Leu)	rs61751443
NM_006940.6(SOX5):c.637C>T (p.Arg213Ter)	rs767241917
Single allele

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