List of variants in gene NBN reported as benign by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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: 13

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HGVS	dbSNP	gnomAD frequency
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.643C>T (p.Arg215Trp)	rs34767364	0.00206
NM_002485.5(NBN):c.283G>A (p.Asp95Asn)	rs61753720	0.00188
NM_002485.5(NBN):c.511A>G (p.Ile171Val)	rs61754966	0.00145
NM_002485.5(NBN):c.1317A>G (p.Ile439Met)	rs28538230	0.00114
NM_002485.5(NBN):c.441C>T (p.Cys147=)	rs137857529	0.00062
NM_002485.5(NBN):c.1720T>A (p.Leu574Ile)	rs142334798	0.00044
NM_002485.5(NBN):c.1690G>A (p.Glu564Lys)	rs72550742	0.00030
NM_002485.5(NBN):c.939G>A (p.Ala313=)	rs145750430	0.00025
NM_002485.5(NBN):c.2220T>C (p.Ala740=)	rs147494981	0.00019
NM_002485.5(NBN):c.1809C>A (p.Phe603Leu)	rs192236678	0.00014
NM_002485.5(NBN):c.1035C>T (p.Gly345=)	rs146605798	0.00011

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