List of variants in gene MEF2C reported as not provided for 5q14.3 microdeletion syndrome

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_002397.5(MEF2C):c.411del (p.Pro138fs)	rs1581753788
NM_002397.5(MEF2C):c.413del (p.Pro138fs)	rs1581753587
NM_002397.5(MEF2C):c.68A>G (p.Lys23Arg)	rs797045053

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