rs879255330

Orientation

plus

Stabilized

plus

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

Make rs879255330(-;-)

Reference

GRCh38.p2 38.2/147

Chromosome

13

Position

32340821

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs879255330
dbSNP (classic)	rs879255330
ClinGen	rs879255330
ebi	rs879255330
HLI	rs879255330
Exac	rs879255330
Gnomad	rs879255330
Varsome	rs879255330
LitVar	rs879255330
Map	rs879255330
PheGenI	rs879255330
Biobank	rs879255330
1000 genomes	rs879255330
hgdp	rs879255330
ensembl	rs879255330
geneview	rs879255330
scholar	rs879255330
google	rs879255330
pharmgkb	rs879255330
gwascentral	rs879255330
openSNP	rs879255330
23andMe	rs879255330
SNPshot	rs879255330
SNPdbe	rs879255330
MSV3d	rs879255330
GWAS Ctlg	rs879255330

Max Magnitude

6

ClinVar
Risk	rs879255330(-;-)
Alt	rs879255330(-;-)
Reference	Rs879255330(TCTC;TCTC)
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.32914958_32914961delTCTC
CLNSRC
CLNACC	RCV000238933.1, RCV000241080.2,