List of variants in gene NBN reported as likely benign by Natera, Inc.

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_002485.5(NBN):c.797C>T (p.Pro266Leu)	rs769420	0.00955
NM_002485.5(NBN):c.2146A>G (p.Asn716Asp)	rs72563785	0.00830
NM_002485.5(NBN):c.1222A>G (p.Lys408Glu)	rs34120922	0.00276
NM_002485.5(NBN):c.441C>T (p.Cys147=)	rs137857529	0.00062
NM_002485.5(NBN):c.896+4T>C	rs190843577	0.00054
NM_002485.5(NBN):c.2202A>G (p.Ala734=)	rs200452212	0.00016
NM_002485.5(NBN):c.1036G>A (p.Val346Met)	rs200297914	0.00011
NM_002485.5(NBN):c.1089C>T (p.Tyr363=)	rs121908974	0.00004
NM_002485.5(NBN):c.415A>G (p.Thr139Ala)	rs543852763	0.00001
NM_002485.5(NBN):c.105T>A (p.Ile35=)	rs78870221
NM_002485.5(NBN):c.1182A>G (p.Arg394=)	rs1586059412
NM_002485.5(NBN):c.2071-8T>C	rs1178683426

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