List of variants in gene FGD4 reported as benign for Charcot-Marie-Tooth disease

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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	gnomAD frequency
NM_001370298.3(FGD4):c.1716G>A (p.Arg572=)	rs10844253	0.27488
NM_001370298.3(FGD4):c.1929G>A (p.Ala643=)	rs11052110	0.25239
NM_001370298.3(FGD4):c.2047-7T>C	rs11052113	0.15104
NM_001370298.3(FGD4):c.1750-12C>T	rs73083501	0.08851
NM_001370298.3(FGD4):c.1404+8G>A	rs12823621	0.07737
NM_001370298.3(FGD4):c.1926T>C (p.Ser642=)	rs60803891	0.01632
NM_001370298.3(FGD4):c.1954-8T>C	rs115061722	0.01466
NM_001370298.3(FGD4):c.1247+10G>T	rs41276676	0.00792
NM_001370298.3(FGD4):c.1971C>T (p.Ile657=)	rs61748364	0.00526
NM_001370298.3(FGD4):c.2122C>A (p.Pro708Thr)	rs144693221
NM_001370298.3(FGD4):c.846C>G (p.Asp282Glu)	rs904582
NM_001370298.3(FGD4):c.846C>T (p.Asp282=)	rs904582

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