List of variants in gene BRCA2 reported as benign for BRCA2-related disorder

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 16

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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.68-7T>A	rs81002830	0.00277
NM_000059.4(BRCA2):c.8182G>A (p.Val2728Ile)	rs28897749	0.00239
NM_000059.4(BRCA2):c.3515C>T (p.Ser1172Leu)	rs80358600	0.00146
NM_000059.4(BRCA2):c.6821G>T (p.Gly2274Val)	rs55712212	0.00126
NM_000059.4(BRCA2):c.4585G>A (p.Gly1529Arg)	rs28897728	0.00044
NM_000059.4(BRCA2):c.4779A>C (p.Glu1593Asp)	rs80358703	0.00013
NM_000059.4(BRCA2):c.1889C>T (p.Thr630Ile)	rs80358479	0.00011
NM_000059.4(BRCA2):c.1662T>G (p.Cys554Trp)	rs80358451	0.00007
NM_000059.4(BRCA2):c.3568C>T (p.Arg1190Trp)	rs80358604	0.00007
NM_000059.4(BRCA2):c.5529A>C (p.Ala1843=)	rs372951842	0.00007
NM_000059.4(BRCA2):c.9592T>C (p.Cys3198Arg)	rs80359229	0.00005
NM_000059.4(BRCA2):c.4570T>G (p.Phe1524Val)	rs56386506	0.00004
NM_000059.4(BRCA2):c.6143A>T (p.Asn2048Ile)	rs80358853	0.00004
NM_000059.4(BRCA2):c.4670C>G (p.Thr1557Ser)	rs80358698	0.00001
NM_000059.4(BRCA2):c.8850G>T (p.Lys2950Asn)	rs28897754

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