rs276174902

Orientation

plus

Stabilized

plus

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

Make rs276174902(G;G)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32332287

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs276174902
dbSNP (classic)	rs276174902
ClinGen	rs276174902
ebi	rs276174902
HLI	rs276174902
Exac	rs276174902
Gnomad	rs276174902
Varsome	rs276174902
LitVar	rs276174902
Map	rs276174902
PheGenI	rs276174902
Biobank	rs276174902
1000 genomes	rs276174902
hgdp	rs276174902
ensembl	rs276174902
geneview	rs276174902
scholar	rs276174902
google	rs276174902
pharmgkb	rs276174902
gwascentral	rs276174902
openSNP	rs276174902
23andMe	rs276174902
SNPshot	rs276174902
SNPdbe	rs276174902
MSV3d	rs276174902
GWAS Ctlg	rs276174902

Max Magnitude

6

rs276174902, also known as S270X, c.809C>G and p.Ser270Ter, is a variant in the BRCA2 gene considered pathogenic for breast cancer in ClinVar.

ClinVar
Risk	rs276174902(G;G)
Alt	rs276174902(G;G)
Reference	Rs276174902(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.32906424C>G
CLNSRC	ClinVar
CLNACC	RCV000045422.2, RCV000112846.3,