List of variants in gene BRCA2 reported as benign by Hereditary Cancer Genetics group, Vall d'Hebron Institute of Oncology

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_000059.4(BRCA2):c.7435+6G>A	rs81002852	0.00053
NM_000059.4(BRCA2):c.7805+13A>G	rs149769332	0.00019
NM_000059.4(BRCA2):c.9501+9A>C	rs81002867	0.00011
NM_000059.4(BRCA2):c.632-16A>C	rs81002905	0.00003
NM_000059.4(BRCA2):c.9501+4A>G	rs81002848	0.00002
NM_000059.4(BRCA2):c.8488-20T>G	rs1593930846
NM_000059.4(BRCA2):c.9257-10dup	rs276174919

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