rs276174862

Orientation

plus

Stabilized

plus

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

Make rs276174862(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32340073

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs276174862
dbSNP (classic)	rs276174862
ClinGen	rs276174862
ebi	rs276174862
HLI	rs276174862
Exac	rs276174862
Gnomad	rs276174862
Varsome	rs276174862
LitVar	rs276174862
Map	rs276174862
PheGenI	rs276174862
Biobank	rs276174862
1000 genomes	rs276174862
hgdp	rs276174862
ensembl	rs276174862
geneview	rs276174862
scholar	rs276174862
google	rs276174862
pharmgkb	rs276174862
gwascentral	rs276174862
openSNP	rs276174862
23andMe	rs276174862
SNPshot	rs276174862
SNPdbe	rs276174862
MSV3d	rs276174862
GWAS Ctlg	rs276174862

Merged from

Rs886038129

Max Magnitude

6

rs276174862 appears to have been merged into rs80359530.

ClinVar
Risk	rs276174862(-;-)
Alt	rs276174862(-;-)
Reference	Rs276174862(CTCT;CTCT)
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.32914212_32914215delCTCT
CLNSRC	Breast Cancer Information Core (BRCA2)
CLNACC	RCV000044727.2, RCV000241138.3,