List of variants in gene MECP2 reported as uncertain significance by Molecular Diagnostics Lab, Nemours Children's Health, Delaware

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_001110792.2(MECP2):c.1096C>T (p.Arg366Cys)	rs143876280	0.00005
NM_001110792.2(MECP2):c.554C>G (p.Pro185Arg)	rs267608492	0.00001
NM_001110792.2(MECP2):c.1134CCA[2] (p.His384del)	rs61752381
NM_001110792.2(MECP2):c.1184T>C (p.Leu395Pro)	rs1060499622
NM_001110792.2(MECP2):c.1191_1244del (p.Leu398_Pro415del)	rs1557135259
NM_001110792.2(MECP2):c.1192_1233del (p.Leu398_Pro411del)	rs267608579
NM_001110792.2(MECP2):c.1216_1251del (p.Glu406_Pro417del)	rs782746707
NM_001110792.2(MECP2):c.349A>C (p.Thr117Pro)	rs1060499623
NM_001110792.2(MECP2):c.433C>T (p.Arg145Cys)	rs28934904
NM_001110792.2(MECP2):c.491C>G (p.Pro164Arg)	rs61748404

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