rs80359725

plus

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

Make rs80359725(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32376713

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs80359725
dbSNP (classic)	rs80359725
ClinGen	rs80359725
ebi	rs80359725
HLI	rs80359725
Exac	rs80359725
Gnomad	rs80359725
Varsome	rs80359725
LitVar	rs80359725
Map	rs80359725
PheGenI	rs80359725
Biobank	rs80359725
1000 genomes	rs80359725
hgdp	rs80359725
ensembl	rs80359725
geneview	rs80359725
scholar	rs80359725
google	rs80359725
pharmgkb	rs80359725
gwascentral	rs80359725
openSNP	rs80359725
23andMe	rs80359725
SNPshot	rs80359725
SNPdbe	rs80359725
MSV3d	rs80359725
GWAS Ctlg	rs80359725

Max Magnitude

6

rs80359725, also known as 8904delA, c.8676_8676delA and p.Arg2892Serfs, is a variant in the BRCA2 gene considered pathogenic for breast cancer in ClinVar.

ClinVar
Risk	rs80359725(-;-)
Alt	rs80359725(-;-)
Reference	Rs80359725(A;A)
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.32950850delA
CLNSRC	Breast Cancer Information Core (BRCA2)
CLNACC	RCV000045599.2, RCV000113986.3,