rs276174875

plus

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

Make rs276174875(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32341028

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs276174875
dbSNP (classic)	rs276174875
ClinGen	rs276174875
ebi	rs276174875
HLI	rs276174875
Exac	rs276174875
Gnomad	rs276174875
Varsome	rs276174875
LitVar	rs276174875
Map	rs276174875
PheGenI	rs276174875
Biobank	rs276174875
1000 genomes	rs276174875
hgdp	rs276174875
ensembl	rs276174875
geneview	rs276174875
scholar	rs276174875
google	rs276174875
pharmgkb	rs276174875
gwascentral	rs276174875
openSNP	rs276174875
23andMe	rs276174875
SNPshot	rs276174875
SNPdbe	rs276174875
MSV3d	rs276174875
GWAS Ctlg	rs276174875

Max Magnitude

6

rs276174875, also known as 6901delA, c.6673_6673delA and p.Thr2225Glnfs, is a variant in the BRCA2 gene considered pathogenic for breast cancer in ClinVar.

ClinVar
Risk	rs276174875(-;-)
Alt	rs276174875(-;-)
Reference	Rs276174875(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.32915165delA
CLNSRC	Breast Cancer Information Core (BRCA2)
CLNACC	RCV000045013.2, RCV000113625.3,