List of variants in gene EGR2 reported as likely benign for Charcot-Marie-Tooth disease

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: 14

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HGVS	dbSNP
NM_000399.5(EGR2):c.-1A>G	rs553201646
NM_000399.5(EGR2):c.1242G>A (p.Lys414=)	rs554456422
NM_000399.5(EGR2):c.1352G>A (p.Gly451Asp)	rs138967272
NM_000399.5(EGR2):c.1352G>T (p.Gly451Val)	rs138967272
NM_000399.5(EGR2):c.1395G>A (p.Pro465=)	rs779811073
NM_000399.5(EGR2):c.210G>A (p.Ser70=)	rs0
NM_000399.5(EGR2):c.222A>C (p.Pro74=)	rs0
NM_000399.5(EGR2):c.222A>G (p.Pro74=)	rs201068734
NM_000399.5(EGR2):c.246C>G (p.Val82=)	rs144217451
NM_000399.5(EGR2):c.645G>A (p.Thr215=)	rs0
NM_000399.5(EGR2):c.774G>A (p.Val258=)	rs0
NM_000399.5(EGR2):c.789T>C (p.Thr263=)	rs0
NM_000399.5(EGR2):c.816C>A (p.Thr272=)	rs863224359
NM_000399.5(EGR2):c.843C>T (p.Thr281=)	rs0

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