List of variants in gene NBN reported as likely benign for idiopathic disease

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: 7

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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.1489A>G (p.Thr497Ala)	rs3026268	0.00711
NM_002485.5(NBN):c.1222A>G (p.Lys408Glu)	rs34120922	0.00276
NM_002485.5(NBN):c.-2C>T	rs202104448	0.00010
NM_002485.5(NBN):c.995-17A>G	rs372875251	0.00002
NM_002485.5(NBN):c.540C>T (p.Phe180=)	rs1060504928

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