List of variants in gene BRCA2 reported as uncertain significance by Soonchunhyang University Bucheon Hospital, Soonchunhyang University Medical Center

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_000059.4(BRCA2):c.964A>C (p.Lys322Gln)	rs11571640	0.00008
NM_000059.4(BRCA2):c.9275A>G (p.Tyr3092Cys)	rs80359195	0.00005
NM_000059.4(BRCA2):c.1744A>C (p.Thr582Pro)	rs80358457	0.00003

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