List of variants in gene BRCA2 reported as likely benign by Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics

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_000059.3(BRCA2):c.5704G>A (p.Asp1902Asn)	rs4987048	0.00655
NM_000059.4(BRCA2):c.4258G>T (p.Asp1420Tyr)	rs28897727	0.00609
NM_000059.4(BRCA2):c.6347A>G (p.His2116Arg)	rs55953736	0.00396
NM_000059.4(BRCA2):c.3869G>A (p.Cys1290Tyr)	rs41293485	0.00307
NM_000059.4(BRCA2):c.1786G>C (p.Asp596His)	rs56328701	0.00025
NM_000059.4(BRCA2):c.9038C>T (p.Thr3013Ile)	rs28897755	0.00022
NM_000059.4(BRCA2):c.5710C>G (p.Leu1904Val)	rs55875643	0.00020
NM_000059.4(BRCA2):c.6325G>A (p.Val2109Ile)	rs79456940	0.00006

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