List of variants in gene combination LOC126860531, NDRG1 reported as uncertain significance for Charcot-Marie-Tooth disease type 4D

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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: 7

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HGVS	dbSNP	gnomAD frequency
NM_006096.4(NDRG1):c.789G>A (p.Ser263=)	rs61755062	0.00102
NM_006096.4(NDRG1):c.731C>T (p.Pro244Leu)	rs748984505	0.00002
NM_006096.4(NDRG1):c.699-3C>T	rs931942837	0.00001
NM_006096.4(NDRG1):c.805G>A (p.Val269Met)	rs750779893	0.00001
NM_006096.4(NDRG1):c.755+1G>A	rs2130692394
NM_006096.4(NDRG1):c.802G>T (p.Ala268Ser)	rs752290896
NM_006096.4(NDRG1):c.807+1G>T

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