List of variants in gene NDRG1 reported as likely 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: 9

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HGVS	dbSNP	gnomAD frequency
NM_006096.4(NDRG1):c.63+1G>A	rs1320417829	0.00001
NM_006096.4(NDRG1):c.326+1G>A	rs1586446057
NM_006096.4(NDRG1):c.450+2_450+3del	rs1856488064
NM_006096.4(NDRG1):c.537+1G>T
NM_006096.4(NDRG1):c.595-2A>T	rs758718584
NM_006096.4(NDRG1):c.808-2A>G	rs112360093
NM_006096.4(NDRG1):c.855+2T>C
NM_006096.4(NDRG1):c.891+2T>C	rs1586407193
NM_006096.4(NDRG1):c.99+1G>A	rs2130785568

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