rs80359102

Orientation

plus

Stabilized

plus

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

Make rs80359102(A;A)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32370972

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs80359102
dbSNP (classic)	rs80359102
ClinGen	rs80359102
ebi	rs80359102
HLI	rs80359102
Exac	rs80359102
Gnomad	rs80359102
Varsome	rs80359102
LitVar	rs80359102
Map	rs80359102
PheGenI	rs80359102
Biobank	rs80359102
1000 genomes	rs80359102
hgdp	rs80359102
ensembl	rs80359102
geneview	rs80359102
scholar	rs80359102
google	rs80359102
pharmgkb	rs80359102
gwascentral	rs80359102
openSNP	rs80359102
23andMe	rs80359102
SNPshot	rs80359102
SNPdbe	rs80359102
MSV3d	rs80359102
GWAS Ctlg	rs80359102

Max Magnitude

6

rs80359102, also known as S2835X, c.8504C>A and p.Ser2835Ter, is a variant in the BRCA2 gene considered pathogenic for breast cancer in ClinVar.

ClinVar
Risk	rs80359102(A;A) rs80359102(G;G)
Alt	rs80359102(A;A) rs80359102(G;G)
Reference	Rs80359102(C;C)
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.32945109C>A; NC_000013.10:g.32945109C>G
CLNSRC	ClinVar
CLNACC	RCV000045541.2, RCV000113951.3, RCV000256554.2,