"Genome-Nilou Lab"[submitter] AND "NDRG1"[gene] - ClinVar - NCBI

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Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 673449	NM_006096.4(NDRG1):c.891+39C>A	NDRG1	Single nucleotide variant (intron variant)	Charcot-Marie-Tooth disease type 4D +1 more	GBenign
Select item 667649	NM_006096.4(NDRG1):c.855+148T>C	NDRG1	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 138434	NM_006096.4(NDRG1):c.756-5C>T	LOC126860531, NDRG1	Single nucleotide variant (intron variant)	Charcot-Marie-Tooth disease type 4 +4 more	GBenign
Select item 138433	NM_006096.4(NDRG1):c.755+10T>C	LOC126860531, NDRG1	Single nucleotide variant (intron variant)	Charcot-Marie-Tooth disease type 4 +4 more	GBenign
Select item 673448	NM_006096.4(NDRG1):c.699-51A>C	LOC126860531, NDRG1	Single nucleotide variant (intron variant)	Charcot-Marie-Tooth disease type 4D +1 more	GBenign
Select item 673388	NM_006096.4(NDRG1):c.698+84A>G	NDRG1	Single nucleotide variant (intron variant)	Charcot-Marie-Tooth disease type 4D +1 more	GBenign
Select item 667643	NM_006096.4(NDRG1):c.538-132G>C	NDRG1	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 670539	NM_006096.4(NDRG1):c.450+61A>G	NDRG1	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 672421	NM_006096.4(NDRG1):c.389+82G>T	NDRG1	Single nucleotide variant (intron variant)	not provided +1 more	GLikely benign
Select item 1185231	NM_006096.4(NDRG1):c.327-33C>T	NDRG1	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 671034	NM_006096.4(NDRG1):c.327-48C>G	NDRG1	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 259916	NM_006096.4(NDRG1):c.64-6T>C	NDRG1	Single nucleotide variant (intron variant)	not provided +4 more	GBenign