List of variants in gene BRCA2 reported by Department of Medical Genetics, University Hospital of North Norway

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_000059.4(BRCA2):c.4068G>A (p.Leu1356=)	rs28897724	0.00295
NM_000059.4(BRCA2):c.68-7T>A	rs81002830	0.00277
NM_000059.4(BRCA2):c.6100C>T (p.Arg2034Cys)	rs1799954	0.00268
NM_000059.4(BRCA2):c.6821G>T (p.Gly2274Val)	rs55712212	0.00126
NM_000059.4(BRCA2):c.2680G>A (p.Val894Ile)	rs28897715	0.00011
NM_000059.4(BRCA2):c.3568C>T (p.Arg1190Trp)	rs80358604	0.00007
NM_000059.4(BRCA2):c.4828G>A (p.Val1610Met)	rs80358705	0.00006
NM_000059.4(BRCA2):c.750G>A (p.Val250=)	rs143214959	0.00005
NM_000059.4(BRCA2):c.7301A>C (p.Lys2434Thr)	rs80358954	0.00003
NM_000059.4(BRCA2):c.40A>G (p.Ile14Val)	rs886038198	0.00001
NM_000059.4(BRCA2):c.8177A>G (p.Tyr2726Cys)	rs80359064	0.00001
NM_000059.4(BRCA2):c.5272_5274del (p.Asn1758del)	rs587780655
NM_000059.4(BRCA2):c.8323A>G (p.Met2775Val)	rs767209209
NM_000059.4(BRCA2):c.9116C>T (p.Pro3039Leu)	rs80359167

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