rs80359344

plus

Geno	Mag	Summary
(-;G)	6	BRCA2 variant considered pathogenic for breast cancer
(G;G)	0	common in clinvar

Make rs80359344(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32337086

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs80359344
dbSNP (classic)	rs80359344
ClinGen	rs80359344
ebi	rs80359344
HLI	rs80359344
Exac	rs80359344
Gnomad	rs80359344
Varsome	rs80359344
LitVar	rs80359344
Map	rs80359344
PheGenI	rs80359344
Biobank	rs80359344
1000 genomes	rs80359344
hgdp	rs80359344
ensembl	rs80359344
geneview	rs80359344
scholar	rs80359344
google	rs80359344
pharmgkb	rs80359344
gwascentral	rs80359344
openSNP	rs80359344
23andMe	rs80359344
SNPshot	rs80359344
SNPdbe	rs80359344
MSV3d	rs80359344
GWAS Ctlg	rs80359344

Max Magnitude

6

rs80359344, also known as 2959delG, c.2731_2731delG and p.Glu911Lysfs, is a variant in the BRCA2 gene considered pathogenic for breast cancer in ClinVar.

ClinVar
Risk	rs80359344(-;-)
Alt	rs80359344(-;-)
Reference	Rs80359344(G;G)
Significance	Pathogenic
Disease	Familial cancer of breast Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32911223delG
CLNSRC	Breast Cancer Information Core (BRCA2)
CLNACC	RCV000044043.2, RCV000113084.2,