Variants in gene BRCA2 with conflicting interpretations "pathogenic" and "benign"

Submission 1 (pathogenic) minimum review status:		Submission 1 (pathogenic) method:
Submission 2 (benign) minimum review status:		Submission 2 (benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 3

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HGVS	dbSNP	gnomAD frequency
NM_000059.4(BRCA2):c.5640T>G (p.Asn1880Lys)	rs11571657	0.00288
NM_000059.4(BRCA2):c.7992T>A (p.Ile2664=)	rs80359800	0.00001
NM_000059.4(BRCA2):c.7879A>T (p.Ile2627Phe)	rs80359014

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