List of variants in gene NBN reported as likely pathogenic for Hereditary breast ovarian cancer syndrome

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_002485.5(NBN):c.175C>T (p.Gln59Ter)	rs1554568427	0.00001
NM_002485.5(NBN):c.156_157del (p.Ser53fs)	rs767454740
NM_002485.5(NBN):c.46_49del (p.Tyr16fs)	rs1812139426

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