List of variants in gene NDRG1 reported as likely benign for Charcot-Marie-Tooth disease type 4D

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: 17

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HGVS	dbSNP	gnomAD frequency
NM_006096.4(NDRG1):c.389+82G>T	rs2233329	0.03173
NM_006096.4(NDRG1):c.*1622T>G	rs7825439	0.02986
NM_006096.4(NDRG1):c.*264C>G	rs73711834	0.02269
NM_006096.4(NDRG1):c.*653T>C	rs147301529	0.01388
NM_006096.4(NDRG1):c.306C>T (p.Gly102=)	rs2233322	0.01251
NM_006096.4(NDRG1):c.507G>A (p.Ala169=)	rs2233331	0.01225
NM_006096.4(NDRG1):c.-18-2_-18-1del	rs371927413	0.00490
NM_006096.4(NDRG1):c.879G>A (p.Pro293=)	rs2233340	0.00458
NM_006096.4(NDRG1):c.331A>C (p.Met111Leu)	rs2233328	0.00201
NM_006096.4(NDRG1):c.*1473G>A	rs187466317	0.00026
NM_006096.4(NDRG1):c.1134G>A (p.Ser378=)	rs750369546	0.00014
NM_006096.4(NDRG1):c.*377G>A	rs377385607	0.00003
NM_006096.4(NDRG1):c.591G>A (p.Gly197=)	rs377257830	0.00001
NM_006096.4(NDRG1):c.855+8G>A	rs776826543	0.00001
NM_006096.4(NDRG1):c.1053_1082del (p.340TRSRSHTSEG[2])	rs751274009
NM_006096.4(NDRG1):c.1077_1106dup (p.340TRSRSHTSEG[4])	rs1554747463
NM_006096.4(NDRG1):c.1092G>A (p.Ser364=)	rs578199680

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