rs80359356

plus

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

Make rs80359356(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32337189

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs80359356
dbSNP (classic)	rs80359356
ClinGen	rs80359356
ebi	rs80359356
HLI	rs80359356
Exac	rs80359356
Gnomad	rs80359356
Varsome	rs80359356
LitVar	rs80359356
Map	rs80359356
PheGenI	rs80359356
Biobank	rs80359356
1000 genomes	rs80359356
hgdp	rs80359356
ensembl	rs80359356
geneview	rs80359356
scholar	rs80359356
google	rs80359356
pharmgkb	rs80359356
gwascentral	rs80359356
openSNP	rs80359356
23andMe	rs80359356
SNPshot	rs80359356
SNPdbe	rs80359356
MSV3d	rs80359356
GWAS Ctlg	rs80359356

Max Magnitude

6

rs80359356, also known as 3062delAA, c.2834_2835delAA and p.Lys945Argfs, is a variant in the BRCA2 gene considered pathogenic for breast cancer in ClinVar.

ClinVar
Risk	rs80359356(-;-)
Alt	rs80359356(-;-)
Reference	Rs80359356(AA;AA)
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.32911326_32911327delAA
CLNSRC	Breast Cancer Information Core (BRCA2)
CLNACC	RCV000049220.2, RCV000113099.3,