List of variants in gene BRCA2 reported as uncertain significance by Centre for Mendelian Genomics, University Medical Centre Ljubljana

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_000059.4(BRCA2):c.10095_10096insT (p.Ser3366Ter)	rs730881599	0.00033
NM_000059.4(BRCA2):c.2063A>G (p.Tyr688Cys)	rs28897713
NM_000059.4(BRCA2):c.3723T>G (p.Phe1241Leu)	rs587782723
NM_000059.4(BRCA2):c.3861TAA[1] (p.Asn1288del)	rs276174837
NM_000059.4(BRCA2):c.7175A>C (p.Lys2392Thr)	rs2072679105
NM_000059.4(BRCA2):c.8415ATC[1] (p.Ser2807del)	rs1060502398
NM_000059.4(BRCA2):c.8507C>T (p.Ser2836Phe)	rs863224599
NM_000059.4(BRCA2):c.9874C>T (p.Pro3292Ser)	rs876660917
NM_000059.4(BRCA2):c.9971C>A (p.Pro3324Gln)	rs1593202112

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