List of variants in gene BRCA2 reported as benign by GeneKor MSA

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: 28

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HGVS	dbSNP	gnomAD frequency
NM_000059.4(BRCA2):c.4563A>G (p.Leu1521=)	rs206075	0.97986
NM_000059.4(BRCA2):c.7806-14T>C	rs9534262	0.53977
NM_000059.4(BRCA2):c.8755-66T>C	rs4942486	0.51824
NM_000059.4(BRCA2):c.631+183T>A	rs3752451	0.32939
NM_000059.4(BRCA2):c.3396A>G (p.Lys1132=)	rs1801406	0.28273
NM_000059.4(BRCA2):c.*369A>G	rs7334543	0.27664
NM_000059.4(BRCA2):c.1114A>C (p.Asn372His)	rs144848	0.23116
NM_000059.4(BRCA2):c.681+56C>T	rs2126042	0.21010
NM_000059.4(BRCA2):c.-26G>A	rs1799943	0.20795
NM_000059.4(BRCA2):c.1910-74T>C	rs2320236	0.19842
NM_000059.4(BRCA2):c.3807T>C (p.Val1269=)	rs543304	0.18381
NM_000059.4(BRCA2):c.*105A>C	rs15869	0.15131
NM_000059.4(BRCA2):c.2971A>G (p.Asn991Asp)	rs1799944	0.04357
NM_000059.4(BRCA2):c.9257-83G>A	rs9595456	0.04317
NM_000059.4(BRCA2):c.425+67A>C	rs11571610	0.03705
NM_000059.4(BRCA2):c.426-89T>C	rs3783265	0.03704
NM_000059.4(BRCA2):c.2229T>C (p.His743=)	rs1801499	0.03698
NM_000059.4(BRCA2):c.1910-51G>T	rs11571651	0.03694
NM_000059.4(BRCA2):c.865A>C (p.Asn289His)	rs766173	0.03693
NM_000059.4(BRCA2):c.1365A>G (p.Ser455=)	rs1801439	0.03688
NM_000059.4(BRCA2):c.7435+53C>T	rs11147489	0.03657
NM_000059.4(BRCA2):c.7397= (p.Val2466=)	rs169547	0.02098
NM_000059.3(BRCA2):c.5704G>A (p.Asp1902Asn)	rs4987048	0.00655
NM_000059.4(BRCA2):c.9976A>T (p.Lys3326Ter)	rs11571833	0.00597
NM_000059.4(BRCA2):c.9649-19G>A	rs11571830	0.00047
NM_000059.4(BRCA2):c.6513G>C (p.Val2171=)	rs206076
NM_000059.4(BRCA2):c.6938-120T>C	rs206080
NM_000059.4(BRCA2):c.7242A>G (p.Ser2414=)	rs1799955

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