List of variants in gene BRCA2 reported as benign for Fanconi anemia complementation group D1

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: 27

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HGVS	dbSNP	gnomAD frequency
NM_000059.4(BRCA2):c.6513G>C (p.Val2171=)	rs206076	0.99779
NM_000059.4(BRCA2):c.4563A>G (p.Leu1521=)	rs206075	0.97986
NM_000059.4(BRCA2):c.7806-14T>C	rs9534262	0.53809
NM_000059.4(BRCA2):c.3396A>G (p.Lys1132=)	rs1801406	0.28273
NM_000059.4(BRCA2):c.*369A>G	rs7334543	0.26990
NM_000059.4(BRCA2):c.1114A>C (p.Asn372His)	rs144848	0.23116
NM_000059.4(BRCA2):c.-26G>A	rs1799943	0.20795
NM_000059.4(BRCA2):c.*532A>G	rs11571836	0.18977
NM_000059.4(BRCA2):c.3807T>C (p.Val1269=)	rs543304	0.18035
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.2229T>C (p.His743=)	rs1801499	0.04095
NM_000059.4(BRCA2):c.1365A>G (p.Ser455=)	rs1801439	0.04091
NM_000059.4(BRCA2):c.10234A>G (p.Ile3412Val)	rs1801426	0.03864
NM_000059.4(BRCA2):c.865A>C (p.Asn289His)	rs766173	0.03693
NM_000059.4(BRCA2):c.5744C>T (p.Thr1915Met)	rs4987117	0.01796
NM_000059.4(BRCA2):c.*397C>A	rs11571835	0.01470
NM_000059.4(BRCA2):c.8460A>C (p.Val2820=)	rs9590940	0.01220
NM_000059.4(BRCA2):c.7319A>G (p.His2440Arg)	rs4986860	0.00910
NM_000059.4(BRCA2):c.5418A>G (p.Glu1806=)	rs34351119	0.00791
NM_000059.4(BRCA2):c.*295C>G	rs11571834	0.00789
NM_000059.4(BRCA2):c.9730G>A (p.Val3244Ile)	rs11571831	0.00725
NM_000059.4(BRCA2):c.1275A>G (p.Glu425=)	rs34355306	0.00324
NM_000059.4(BRCA2):c.5312G>A (p.Gly1771Asp)	rs80358755	0.00021
NM_000059.4(BRCA2):c.964A>C (p.Lys322Gln)	rs11571640	0.00008
NM_000059.4(BRCA2):c.6131G>T (p.Gly2044Val)	rs56191579	0.00001
NM_000059.4(BRCA2):c.7242A>G (p.Ser2414=)	rs1799955

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