List of variants in gene MECP2 reported as benign for History of neurodevelopmental disorder

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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: 12

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HGVS	dbSNP	gnomAD frequency
NM_001110792.2(MECP2):c.1269C>T (p.Ser423=)	rs3027928	0.01726
NM_001110792.2(MECP2):c.1225G>A (p.Glu409Lys)	rs56268439	0.00308
NM_001110792.2(MECP2):c.719C>G (p.Thr240Ser)	rs61749738	0.00291
NM_001110792.2(MECP2):c.1371G>A (p.Thr457=)	rs3027927	0.00256
NM_001110792.2(MECP2):c.618C>T (p.Ser206=)	rs61749711	0.00189
NM_001110792.2(MECP2):c.1071A>G (p.Lys357=)	rs61752362	0.00157
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.*9G>A	rs144008995	0.00080
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.1173C>T (p.Pro391=)	rs61752980	0.00020

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