List of variants reported as uncertain significance for Charcot-Marie-Tooth disease type 4D by Fulgent Genetics, Fulgent Genetics

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_006096.4(NDRG1):c.122A>G (p.His41Arg)	rs2233318	0.00054
NM_006096.4(NDRG1):c.686A>G (p.Asn229Ser)	rs137993172	0.00024
NM_006096.4(NDRG1):c.1109C>G (p.Ala370Gly)	rs367925853
NM_006096.4(NDRG1):c.1109C>T (p.Ala370Val)	rs367925853
NM_006096.4(NDRG1):c.980G>A (p.Arg327His)	rs565705964

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