List of variants in gene MEF2C reported as benign by GeneDx

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: 27

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HGVS	dbSNP	gnomAD frequency
NM_002397.5(MEF2C):c.403-139A>G	rs2247885	0.48476
NM_002397.5(MEF2C):c.-142-333_-142-332insAG	rs10689049	0.42870
NM_001131005.2(MEF2C):c.-239-236T>C	rs17560407	0.18550
NM_002397.5(MEF2C):c.590-95G>T	rs10514303	0.05491
NM_002397.5(MEF2C):c.810+199T>A	rs45563631	0.04734
NM_002397.5(MEF2C):c.810+268C>T	rs72771875	0.02647
NM_002397.5(MEF2C):c.258+155T>G	rs3850650	0.02169
NM_002397.5(MEF2C):c.811-290T>C	rs73773730	0.01835
NM_002397.5(MEF2C):c.811-13C>T	rs201988423	0.00113
NM_002397.5(MEF2C):c.834+15C>T	rs140447603	0.00093
NM_002397.5(MEF2C):c.811-12G>A	rs149706617	0.00064
NM_002397.5(MEF2C):c.402+16A>G	rs373582392	0.00050
NM_001131005.2(MEF2C):c.-143+6T>C	rs749992711	0.00027
NM_002397.5(MEF2C):c.*16C>G	rs200087574	0.00023
NM_002397.5(MEF2C):c.642C>T (p.Asn214=)	rs79455305	0.00019
NM_002397.5(MEF2C):c.-42T>C	rs371238107	0.00018
NM_002397.5(MEF2C):c.180C>T (p.Thr60=)	rs773278207	0.00010
NM_002397.5(MEF2C):c.363C>T (p.Asn121=)	rs186648089	0.00008
NM_002397.5(MEF2C):c.1332C>T (p.His444=)	rs376439815	0.00004
NM_002397.5(MEF2C):c.312C>T (p.Asp104=)	rs587781034	0.00004
NM_002397.5(MEF2C):c.402+208A>G	rs764312143	0.00003
NM_002397.4(MEF2C):c.-450dup	rs144197632
NM_002397.5(MEF2C):c.*32del	rs56660854
NM_002397.5(MEF2C):c.-143+89A>G	rs10044342
NM_002397.5(MEF2C):c.403-211A>G	rs647983
NM_002397.5(MEF2C):c.810+191dup	rs11439565
NM_002397.5(MEF2C):c.834+182del	rs34297769

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