List of variants in gene combination NRL, PCK2 reported as benign by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_004563.4(PCK2):c.372T>C (p.Pro124=)	rs2229661	0.02789
NM_004563.4(PCK2):c.1230A>G (p.Lys410=)	rs2301336	0.02556
NM_004563.4(PCK2):c.6C>T (p.Ala2=)	rs77298044	0.02238
NM_001354768.3(NRL):c.-28+11222A>G	rs190213824	0.00228

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