rs878853302

Orientation

plus

Stabilized

plus

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

Make rs878853302(-;-)

Reference

GRCh38.p2 38.2/147

Chromosome

13

Position

32341180

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs878853302
dbSNP (classic)	rs878853302
ClinGen	rs878853302
ebi	rs878853302
HLI	rs878853302
Exac	rs878853302
Gnomad	rs878853302
Varsome	rs878853302
LitVar	rs878853302
Map	rs878853302
PheGenI	rs878853302
Biobank	rs878853302
1000 genomes	rs878853302
hgdp	rs878853302
ensembl	rs878853302
geneview	rs878853302
scholar	rs878853302
google	rs878853302
pharmgkb	rs878853302
gwascentral	rs878853302
openSNP	rs878853302
23andMe	rs878853302
SNPshot	rs878853302
SNPdbe	rs878853302
MSV3d	rs878853302
GWAS Ctlg	rs878853302

Max Magnitude

6

ClinVar
Risk	rs878853302(-;-)
Alt	rs878853302(-;-)
Reference	Rs878853302(G;G)
Significance	Pathogenic
Disease	Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32915317delG
CLNSRC
CLNACC	RCV000225578.2,