List of variants in gene BRCA2 reported as pathogenic by Equipe Genetique des Anomalies du Developpement, Université de Bourgogne

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_000059.4(BRCA2):c.5946del (p.Ser1982fs)	rs80359550	0.00017
NM_000059.4(BRCA2):c.9294C>G (p.Tyr3098Ter)	rs80359200	0.00002
NM_000059.4(BRCA2):c.2175dup (p.Val726fs)	rs276174819
NM_000059.4(BRCA2):c.3172A>T (p.Lys1058Ter)	rs730881521
NM_000059.4(BRCA2):c.9294C>A (p.Tyr3098Ter)	rs80359200

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