List of variants in gene BRCA2 reported as benign by Pathway Genomics

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: 14

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HGVS	dbSNP	gnomAD frequency
NM_000059.4(BRCA2):c.8830A>T (p.Ile2944Phe)	rs4987047	0.01281
NM_000059.4(BRCA2):c.7319A>G (p.His2440Arg)	rs4986860	0.00984
NM_000059.4(BRCA2):c.7469T>C (p.Ile2490Thr)	rs11571707	0.00868
NM_000059.4(BRCA2):c.8851G>A (p.Ala2951Thr)	rs11571769	0.00809
NM_000059.4(BRCA2):c.7017G>C (p.Lys2339Asn)	rs45574331	0.00792
NM_000059.4(BRCA2):c.7008-62A>G	rs76584943	0.00439
NM_000059.4(BRCA2):c.3869G>A (p.Cys1290Tyr)	rs41293485	0.00307
NM_000059.4(BRCA2):c.6323G>A (p.Arg2108His)	rs35029074	0.00260
NM_000059.4(BRCA2):c.8503T>C (p.Ser2835Pro)	rs11571746	0.00202
NM_000059.4(BRCA2):c.125A>G (p.Tyr42Cys)	rs4987046	0.00158
NM_000059.4(BRCA2):c.8149G>T (p.Ala2717Ser)	rs28897747	0.00127
NM_000059.4(BRCA2):c.10121C>T (p.Thr3374Ile)	rs56309455	0.00059
NM_000059.4(BRCA2):c.6853A>G (p.Ile2285Val)	rs56272235	0.00026
NM_000059.4(BRCA2):c.7057G>C (p.Gly2353Arg)	rs80358935	0.00006

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