List of variants in gene NBN reported by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_002485.5(NBN):c.1197T>C (p.Asp399=)	rs709816	0.51063
NM_002485.5(NBN):c.102G>A (p.Leu34=)	rs1063045	0.32752
NM_002485.5(NBN):c.1915-7A>G	rs2308962	0.32733
NM_002485.5(NBN):c.553G>C (p.Glu185Gln)	rs1805794	0.30329
NM_002485.5(NBN):c.2016A>G (p.Pro672=)	rs1061302	0.30090
NM_002485.5(NBN):c.381T>C (p.Ala127=)	rs61754795	0.00266
NM_002485.5(NBN):c.127C>T (p.Arg43Ter)	rs200287925	0.00006
NM_002485.5(NBN):c.657_661del (p.Lys219fs)	rs587776650

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