List of variants in gene MECP2 reported as likely benign for X-linked disease

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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: 15

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HGVS	dbSNP	gnomAD frequency
NM_001110792.2(MECP2):c.1225G>A (p.Glu409Lys)	rs56268439	0.00308
NM_001110792.2(MECP2):c.638C>T (p.Ala213Val)	rs61748381	0.00150
NM_001110792.2(MECP2):c.246C>T (p.Ser82=)	rs61754439	0.00119
NM_001110792.2(MECP2):c.626C>T (p.Thr209Met)	rs61749714	0.00064
NM_001110792.2(MECP2):c.623C>G (p.Thr208Ser)	rs61749713	0.00034
NM_001110792.2(MECP2):c.978C>T (p.Ile326=)	rs61751446	0.00034
NM_001110792.2(MECP2):c.1174G>A (p.Val392Met)	rs267608572	0.00022
NM_001110792.2(MECP2):c.1293C>T (p.Pro431=)	rs199540575	0.00015
NM_001110792.2(MECP2):c.1409G>A (p.Arg470His)	rs185957513	0.00015
NM_001110792.2(MECP2):c.1196C>T (p.Pro399Leu)	rs63390262	0.00010
NM_001110792.2(MECP2):c.1302C>T (p.Gly434=)	rs61753970	0.00004
NM_001110792.2(MECP2):c.838C>T (p.Arg280Trp)	rs61750239	0.00004
NM_001110792.2(MECP2):c.1241C>T (p.Pro414Leu)	rs61753014
NM_001110792.2(MECP2):c.1351G>A (p.Ala451Thr)	rs61753973
NM_001110792.2(MECP2):c.641C>T (p.Ala214Val)	rs587783138

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