List of variants in gene BRCA2 reported as likely benign by Pathway Genomics

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: 15

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HGVS	dbSNP	gnomAD frequency
NM_000059.4(BRCA2):c.5744C>T (p.Thr1915Met)	rs4987117	0.01834
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.2960A>T (p.Asn987Ile)	rs2227944	0.00356
NM_000059.4(BRCA2):c.68-7T>A	rs81002830	0.00277
NM_000059.4(BRCA2):c.6100C>T (p.Arg2034Cys)	rs1799954	0.00268
NM_000059.4(BRCA2):c.8182G>A (p.Val2728Ile)	rs28897749	0.00239
NM_000059.4(BRCA2):c.7150C>A (p.Gln2384Lys)	rs55977008	0.00203
NM_000059.4(BRCA2):c.4187A>G (p.Gln1396Arg)	rs55969723	0.00168
NM_000059.4(BRCA2):c.8567A>C (p.Glu2856Ala)	rs11571747	0.00158
NM_000059.4(BRCA2):c.2138A>T (p.Gln713Leu)	rs55816687	0.00138
NM_000059.4(BRCA2):c.4585G>A (p.Gly1529Arg)	rs28897728	0.00044
NM_000059.4(BRCA2):c.5785A>G (p.Ile1929Val)	rs79538375	0.00031
NM_000059.4(BRCA2):c.7052C>G (p.Ala2351Gly)	rs80358932	0.00005
NM_000059.4(BRCA2):c.10095delinsGAATTATATCT (p.Ser3366fs)	rs276174803

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