List of variants in gene BRCA2 reported as likely pathogenic by Institute for Clinical Genetics, University Hospital TU Dresden, University Hospital TU Dresden

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: 4

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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.517G>C (p.Gly173Arg)	rs397507768
NM_000059.4(BRCA2):c.7753G>A (p.Gly2585Arg)	rs80359002
NM_000059.4(BRCA2):c.8486A>G (p.Gln2829Arg)	rs80359100

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