rs878853300

Orientation

plus

Stabilized

plus

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

Make rs878853300(-;-)

Reference

GRCh38.p2 38.2/147

Chromosome

13

Position

32340943

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs878853300
dbSNP (classic)	rs878853300
ClinGen	rs878853300
ebi	rs878853300
HLI	rs878853300
Exac	rs878853300
Gnomad	rs878853300
Varsome	rs878853300
LitVar	rs878853300
Map	rs878853300
PheGenI	rs878853300
Biobank	rs878853300
1000 genomes	rs878853300
hgdp	rs878853300
ensembl	rs878853300
geneview	rs878853300
scholar	rs878853300
google	rs878853300
pharmgkb	rs878853300
gwascentral	rs878853300
openSNP	rs878853300
23andMe	rs878853300
SNPshot	rs878853300
SNPdbe	rs878853300
MSV3d	rs878853300
GWAS Ctlg	rs878853300

Max Magnitude

6

ClinVar
Risk	rs878853300(-;-)
Alt	rs878853300(-;-)
Reference	Rs878853300(AA;AA)
Significance	Pathogenic
Disease	Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32915080_32915081delAA
CLNSRC
CLNACC	RCV000225666.2,