List of variants in gene NDRG1 reported as pathogenic by Invitae

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.16C>T (p.Gln6Ter)	rs1048918488	0.00001
NM_006096.4(NDRG1):c.205+1G>A	rs1060503092	0.00001
NM_006096.4(NDRG1):c.442C>T (p.Arg148Ter)	rs119483085	0.00001
NC_000008.10:g.(?_134260948)_(134262796_?)del
NC_000008.10:g.(?_134292465)_(134296564_?)del
NM_006096.4(NDRG1):c.205+1G>C
NM_006096.4(NDRG1):c.205+1G>T	rs1060503092
NM_006096.4(NDRG1):c.205+2T>A	rs1586451553
NM_006096.4(NDRG1):c.330C>G (p.Tyr110Ter)
NM_006096.4(NDRG1):c.368del (p.Pro123fs)	rs2130727371
NM_006096.4(NDRG1):c.40A>T (p.Lys14Ter)
NM_006096.4(NDRG1):c.510_511insTGTGTGGA (p.Gly171fs)
NM_006096.4(NDRG1):c.518_521dup (p.Trp175fs)	rs2130719686
NM_006096.4(NDRG1):c.524G>A (p.Trp175Ter)
NM_006096.4(NDRG1):c.525G>A (p.Trp175Ter)
NM_006096.4(NDRG1):c.604C>T (p.Gln202Ter)	rs1855957969
NM_006096.4(NDRG1):c.641del (p.His214fs)

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