List of variants in gene FGD4 reported as 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: 12

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HGVS	dbSNP
NM_139241.3(FGD4):c.1305G>A (p.Arg435=)	rs10844253
NM_139241.3(FGD4):c.1339-12C>T	rs73083501
NM_139241.3(FGD4):c.1515T>C (p.Ser505=)	rs60803891
NM_139241.3(FGD4):c.1518G>A (p.Ala506=)	rs11052110
NM_139241.3(FGD4):c.1543-8T>C	rs115061722
NM_139241.3(FGD4):c.1560C>T (p.Ile520=)	rs61748364
NM_139241.3(FGD4):c.1636-7T>C	rs11052113
NM_139241.3(FGD4):c.1711C>A (p.Pro571Thr)	rs144693221
NM_139241.3(FGD4):c.435C>G (p.Asp145Glu)	rs904582
NM_139241.3(FGD4):c.435C>T (p.Asp145=)	rs904582
NM_139241.3(FGD4):c.836+10G>T	rs41276676
NM_139241.3(FGD4):c.993+8G>A	rs12823621

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