rs878853298

Orientation

plus

Stabilized

plus

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

Make rs878853298(-;-)

Reference

GRCh38.p2 38.2/147

Chromosome

13

Position

32333384

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs878853298
dbSNP (classic)	rs878853298
ClinGen	rs878853298
ebi	rs878853298
HLI	rs878853298
Exac	rs878853298
Gnomad	rs878853298
Varsome	rs878853298
LitVar	rs878853298
Map	rs878853298
PheGenI	rs878853298
Biobank	rs878853298
1000 genomes	rs878853298
hgdp	rs878853298
ensembl	rs878853298
geneview	rs878853298
scholar	rs878853298
google	rs878853298
pharmgkb	rs878853298
gwascentral	rs878853298
openSNP	rs878853298
23andMe	rs878853298
SNPshot	rs878853298
SNPdbe	rs878853298
MSV3d	rs878853298
GWAS Ctlg	rs878853298

Max Magnitude

6

ClinVar
Risk	rs878853298(-;-)
Alt	rs878853298(-;-)
Reference	Rs878853298(T;T)
Significance	Pathogenic
Disease	Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32907521delT
CLNSRC
CLNACC	RCV000225650.2,