List of variants in gene BRCA2 reported as uncertain significance for adenocarcinoma

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.7397T>C (p.Val2466Ala)	rs169547	0.97902
NM_000059.4(BRCA2):c.1114A>C (p.Asn372His)	rs144848	0.23116
NM_000059.4(BRCA2):c.4376A>G (p.Asn1459Ser)	rs117187202	0.00001
NM_000059.4(BRCA2):c.3858_3860del (p.Lys1286del)	rs80359406

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