List of variants in gene BRCA2 reported as likely benign by Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_000059.4(BRCA2):c.122C>T (p.Pro41Leu)	rs786201716	0.00001
NM_000059.4(BRCA2):c.10102T>C (p.Ser3368Pro)	rs786205482
NM_000059.4(BRCA2):c.8954-5_8954-2del	rs587782878

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