Variants with conflicting interpretations "likely benign" from Women's Health and Genetics/Laboratory Corporation of America, LabCorp and "benign" from RettBASE

Minimum review status of the submission from Women's Health and Genetics/Laboratory Corporation of America, LabCorp:		Collection method of the submission from Women's Health and Genetics/Laboratory Corporation of America, LabCorp:
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Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 4

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HGVS	dbSNP	gnomAD frequency
NM_001110792.2(MECP2):c.669G>C (p.Arg223Ser)	rs61749731	0.00012
NM_001110792.2(MECP2):c.756C>T (p.Thr252=)	rs61749746	0.00009
NM_001110792.2(MECP2):c.1111T>C (p.Ser371Pro)	rs61752371	0.00005
NM_001110792.2(MECP2):c.1169C>T (p.Ala390Val)	rs201314910

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