rs276174838

plus

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

Make rs276174838(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32338294

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs276174838
dbSNP (classic)	rs276174838
ClinGen	rs276174838
ebi	rs276174838
HLI	rs276174838
Exac	rs276174838
Gnomad	rs276174838
Varsome	rs276174838
LitVar	rs276174838
Map	rs276174838
PheGenI	rs276174838
Biobank	rs276174838
1000 genomes	rs276174838
hgdp	rs276174838
ensembl	rs276174838
geneview	rs276174838
scholar	rs276174838
google	rs276174838
pharmgkb	rs276174838
gwascentral	rs276174838
openSNP	rs276174838
23andMe	rs276174838
SNPshot	rs276174838
SNPdbe	rs276174838
MSV3d	rs276174838
GWAS Ctlg	rs276174838

Max Magnitude

6

rs276174838, also known as 4167delC, c.3939delC and p.Tyr1313Terfs, is a variant in the BRCA2 gene considered pathogenic for breast cancer in ClinVar.

23andMe name: i5009151

ClinVar
Risk	rs276174838(-;-)
Alt	rs276174838(-;-)
Reference	Rs276174838(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.32912431delC
CLNSRC	Breast Cancer Information Core (BRCA2)
CLNACC	RCV000044318.2, RCV000113247.2,