rs879255306

Orientation

plus

Stabilized

plus

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

Make rs879255306(-;-)

Reference

GRCh38.p2 38.2/147

Chromosome

13

Position

32346869

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs879255306
dbSNP (classic)	rs879255306
ClinGen	rs879255306
ebi	rs879255306
HLI	rs879255306
Exac	rs879255306
Gnomad	rs879255306
Varsome	rs879255306
LitVar	rs879255306
Map	rs879255306
PheGenI	rs879255306
Biobank	rs879255306
1000 genomes	rs879255306
hgdp	rs879255306
ensembl	rs879255306
geneview	rs879255306
scholar	rs879255306
google	rs879255306
pharmgkb	rs879255306
gwascentral	rs879255306
openSNP	rs879255306
23andMe	rs879255306
SNPshot	rs879255306
SNPdbe	rs879255306
MSV3d	rs879255306
GWAS Ctlg	rs879255306

Max Magnitude

6

ClinVar
Risk	rs879255306(-;-)
Alt	rs879255306(-;-)
Reference	Rs879255306(T;T)
Significance	Pathogenic
Disease	Breast-ovarian cancer not provided
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2 not provided
Reversed	0
HGVS	NC_000013.10:g.32921006delT
CLNSRC
CLNACC	RCV000238627.2, RCV000482674.1,