rs80359205

Orientation

plus

Stabilized

plus

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

Make rs80359205(A;A)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32394749

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs80359205
dbSNP (classic)	rs80359205
ClinGen	rs80359205
ebi	rs80359205
HLI	rs80359205
Exac	rs80359205
Gnomad	rs80359205
Varsome	rs80359205
LitVar	rs80359205
Map	rs80359205
PheGenI	rs80359205
Biobank	rs80359205
1000 genomes	rs80359205
hgdp	rs80359205
ensembl	rs80359205
geneview	rs80359205
scholar	rs80359205
google	rs80359205
pharmgkb	rs80359205
gwascentral	rs80359205
openSNP	rs80359205
23andMe	rs80359205
SNPshot	rs80359205
SNPdbe	rs80359205
MSV3d	rs80359205
GWAS Ctlg	rs80359205

Max Magnitude

6

rs80359205, also known as W3106X, c.9317G>A and p.Trp3106Ter, is a variant in the BRCA2 gene considered pathogenic for breast cancer in ClinVar.

ClinVar
Risk	rs80359205(A;A)
Alt	rs80359205(A;A)
Reference	Rs80359205(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.32968886G>A
CLNSRC	ClinVar
CLNACC	RCV000045792.2, RCV000114090.3,