rs276174900

Orientation

plus

Stabilized

plus

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

Make rs276174900(T;T)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32363204

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs276174900
dbSNP (old)	rs276174900
ClinGen	rs276174900
ebi	rs276174900
HLI	rs276174900
Exac	rs276174900
Gnomad	rs276174900
Varsome	rs276174900
Map	rs276174900
PheGenI	rs276174900
Biobank	rs276174900
1000 genomes	rs276174900
hgdp	rs276174900
ensembl	rs276174900
gopubmed	rs276174900
geneview	rs276174900
scholar	rs276174900
google	rs276174900
pharmgkb	rs276174900
gwascentral	rs276174900
openSNP	rs276174900
23andMe	rs276174900
23andMe all	rs276174900
SNP Nexus
SNPshot	rs276174900
SNPdbe	rs276174900
MSV3d	rs276174900
GWAS Ctlg	rs276174900

Max Magnitude

6

rs276174900, also known as A2668X, c.8002A>T and p.Arg2668Ter, is a variant in the BRCA2 gene considered pathogenic for breast cancer in ClinVar.

ClinVar
Risk	rs276174900(G;G) rs276174900(T;T)
Alt	rs276174900(G;G) rs276174900(T;T)
Reference	Rs276174900(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.32937341A>T
CLNSRC	ClinVar
CLNACC	RCV000045382.2, RCV000113855.3,