rs878853569

Orientation

plus

Stabilized

plus

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

Make rs878853569(GA;GA)

Reference

GRCh38.p2 38.2/147

Chromosome

13

Position

32337837

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs878853569
dbSNP (classic)	rs878853569
ClinGen	rs878853569
ebi	rs878853569
HLI	rs878853569
Exac	rs878853569
Gnomad	rs878853569
Varsome	rs878853569
LitVar	rs878853569
Map	rs878853569
PheGenI	rs878853569
Biobank	rs878853569
1000 genomes	rs878853569
hgdp	rs878853569
ensembl	rs878853569
geneview	rs878853569
scholar	rs878853569
google	rs878853569
pharmgkb	rs878853569
gwascentral	rs878853569
openSNP	rs878853569
23andMe	rs878853569
SNPshot	rs878853569
SNPdbe	rs878853569
MSV3d	rs878853569
GWAS Ctlg	rs878853569

Max Magnitude

6

ClinVar
Risk	rs878853569(AG;AG)
Alt	rs878853569(AG;AG)
Reference	Rs878853569(-;-)
Significance	Pathogenic
Disease	Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32911973_32911974dupGA
CLNSRC
CLNACC	RCV000234119.2, RCV000256803.2,