List of variants in gene BRCA2 reported as likely benign by Eurofins NTD LLC (GA)

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: 23

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HGVS	dbSNP	gnomAD frequency
NM_000059.4(BRCA2):c.68-7T>A	rs81002830	0.00277
NM_000059.4(BRCA2):c.125A>G (p.Tyr42Cys)	rs4987046	0.00158
NM_000059.4(BRCA2):c.8567A>C (p.Glu2856Ala)	rs11571747	0.00158
NM_000059.4(BRCA2):c.9634G>C (p.Gly3212Arg)	rs55775473	0.00141
NM_000059.4(BRCA2):c.2138A>T (p.Gln713Leu)	rs55816687	0.00138
NM_000059.4(BRCA2):c.10110G>A (p.Arg3370=)	rs28897762	0.00132
NM_000059.4(BRCA2):c.1040A>G (p.Gln347Arg)	rs55800493	0.00109
NM_000059.4(BRCA2):c.9235G>A (p.Val3079Ile)	rs55933907	0.00106
NM_000059.4(BRCA2):c.2883G>A (p.Gln961=)	rs11571655	0.00097
NM_000059.4(BRCA2):c.-15A>C	rs138705202	0.00066
NM_000059.4(BRCA2):c.10121C>T (p.Thr3374Ile)	rs56309455	0.00059
NM_000059.4(BRCA2):c.4071A>C (p.Leu1357=)	rs140556653	0.00059
NM_000059.4(BRCA2):c.2145A>G (p.Gly715=)	rs112566179	0.00056
NM_000059.4(BRCA2):c.1964C>G (p.Pro655Arg)	rs28897712	0.00054
NM_000059.4(BRCA2):c.2803G>A (p.Asp935Asn)	rs28897716	0.00054
NM_000059.4(BRCA2):c.9843A>G (p.Pro3281=)	rs11571832	0.00047
NM_000059.4(BRCA2):c.5785A>G (p.Ile1929Val)	rs79538375	0.00031
NM_000059.4(BRCA2):c.1395A>C (p.Val465=)	rs11571641	0.00026
NM_000059.4(BRCA2):c.1786G>C (p.Asp596His)	rs56328701	0.00025
NM_000059.4(BRCA2):c.1123C>T (p.Pro375Ser)	rs80358408	0.00019
NM_000059.4(BRCA2):c.4061C>T (p.Thr1354Met)	rs80358656	0.00014
NM_000059.4(BRCA2):c.1909+9_1909+10del	rs527732001
NM_000059.4(BRCA2):c.8850G>T (p.Lys2950Asn)	rs28897754

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