List of variants in gene BRCA2 reported as pathogenic by Rady Children's Institute for Genomic Medicine, Rady Children's Hospital San Diego

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_000059.4(BRCA2):c.5946del (p.Ser1982fs)	rs80359550	0.00019
NM_000059.4(BRCA2):c.3680_3681del (p.Leu1227fs)	rs80359395	0.00003
NM_000059.4(BRCA2):c.1408dup (p.Glu470fs)	rs80359284
NM_000059.4(BRCA2):c.3751dup (p.Thr1251fs)	rs397507683
NM_000059.4(BRCA2):c.4947_4948del (p.Pro1651fs)	rs80359474
NM_000059.4(BRCA2):c.4965C>A (p.Tyr1655Ter)	rs80358721
NM_000059.4(BRCA2):c.5217_5223del (p.Thr1738_Tyr1739insTer)	rs80359496
NM_000059.4(BRCA2):c.5410_5411del (p.Val1804fs)	rs80359512
NM_000059.4(BRCA2):c.658_659del (p.Val220fs)	rs80359604
NM_000059.4(BRCA2):c.9593_9594del (p.Cys3198fs)	rs1566260198

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