List of variants in gene MECP2 reported as likely benign by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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

Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_001110792.2(MECP2):c.1174G>A (p.Val392Met)	rs267608572	0.00022
NM_001110792.2(MECP2):c.669G>C (p.Arg223Ser)	rs61749731	0.00012
NM_001110792.2(MECP2):c.1196C>T (p.Pro399Leu)	rs63390262	0.00010
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.877G>A (p.Ala293Thr)	rs782239416	0.00004
NM_001110792.2(MECP2):c.968C>T (p.Thr323Met)	rs61751445	0.00003
NM_001110792.2(MECP2):c.414-6C>G	rs782482746	0.00002
NM_001110792.2(MECP2):c.1017C>T (p.Thr339=)	rs1015722593	0.00001
NM_001110792.2(MECP2):c.1169C>T (p.Ala390Val)	rs201314910
NM_001110792.2(MECP2):c.528C>T (p.Ser176=)	rs1557136964
NM_001110792.2(MECP2):c.550C>A (p.Pro184Thr)	rs61748426
NM_001110792.2(MECP2):c.786C>G (p.Arg262=)	rs61748424

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