List of variants in gene MEF2C reported as uncertain significance for not specified

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: 8

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_002397.5(MEF2C):c.1207A>G (p.Thr403Ala)	rs753002290	0.00010
NM_002397.5(MEF2C):c.980G>C (p.Ser327Thr)	rs796052726	0.00005
NM_002397.5(MEF2C):c.531G>A (p.Leu177=)	rs371858773	0.00001
NM_002397.5(MEF2C):c.-208del	rs886060864
NM_002397.5(MEF2C):c.120_125dup (p.Asp40_Cys41dup)	rs796052732
NM_002397.5(MEF2C):c.402+153dup	rs796052736
NM_002397.5(MEF2C):c.826C>G (p.Leu276Val)	rs2152250513
NM_002397.5(MEF2C):c.93G>T (p.Lys31Asn)	rs1057518382

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.