List of variants in gene BRCA2 reported as pathogenic by ClinGen ENIGMA BRCA1 and BRCA2 Variant Curation Expert Panel, ClinGen

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_000059.4(BRCA2):c.5946del (p.Ser1982fs)	rs80359550	0.00017
NM_000059.4(BRCA2):c.6859A>T (p.Arg2287Ter)	rs876661261	0.00001
NM_000059.4(BRCA2):c.7879A>T (p.Ile2627Phe)	rs80359014	0.00001
NM_000059.4(BRCA2):c.9117G>A (p.Pro3039=)	rs28897756	0.00001
NM_000059.4(BRCA2):c.7977-1G>C	rs81002874
NM_000059.4(BRCA2):c.8023A>G (p.Ile2675Val)	rs397507954
NM_000059.4(BRCA2):c.8168A>C (p.Asp2723Ala)	rs41293513
NM_000059.4(BRCA2):c.9227G>T (p.Gly3076Val)	rs80359187

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