List of variants in gene BRCA2 reported as likely pathogenic by Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital

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.8009C>T (p.Ser2670Leu)	rs80359035	0.00001
NM_000059.4(BRCA2):c.8351G>A (p.Arg2784Gln)	rs80359076	0.00001
NM_000059.4(BRCA2):c.2361_2362dup (p.Gly788fs)	rs2548523705
NM_000059.4(BRCA2):c.3426del (p.Phe1142fs)
NM_000059.4(BRCA2):c.4578dup (p.Ala1527fs)
NM_000059.4(BRCA2):c.5206_5207del (p.Gln1736fs)	rs2548530211
NM_000059.4(BRCA2):c.7964A>G (p.Gln2655Arg)	rs80359024
NM_000059.4(BRCA2):c.8331+2T>C	rs398122602
NM_000059.4(BRCA2):c.8754+3G>C	rs397508007

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