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

Submission 1 (benign) minimum review status:		Submission 1 (benign) 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: 11

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HGVS	dbSNP	gnomAD frequency
NM_000059.4(BRCA2):c.1114A>C (p.Asn372His)	rs144848	0.23116
NM_000059.4(BRCA2):c.2971A>G (p.Asn991Asp)	rs1799944	0.04357
NM_000059.4(BRCA2):c.10234A>G (p.Ile3412Val)	rs1801426	0.03864
NM_000059.4(BRCA2):c.865A>C (p.Asn289His)	rs766173	0.03693
NM_000059.4(BRCA2):c.5744C>T (p.Thr1915Met)	rs4987117	0.01834
NM_000059.4(BRCA2):c.8830A>T (p.Ile2944Phe)	rs4987047	0.01281
NM_000059.4(BRCA2):c.8851G>A (p.Ala2951Thr)	rs11571769	0.00809
NM_000059.4(BRCA2):c.4258G>T (p.Asp1420Tyr)	rs28897727	0.00609
NM_000059.4(BRCA2):c.9976A>T (p.Lys3326Ter)	rs11571833	0.00597
NM_000059.4(BRCA2):c.6100C>T (p.Arg2034Cys)	rs1799954	0.00268
NM_000059.4(BRCA2):c.2350A>G (p.Met784Val)	rs11571653	0.00018

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