rs587779364

Orientation

plus

Stabilized

plus

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

Make rs587779364(C;C)

Reference

GRCh38.p2 38.2/144

Chromosome

13

Position

32339719

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs587779364
dbSNP (classic)	rs587779364
ClinGen	rs587779364
ebi	rs587779364
HLI	rs587779364
Exac	rs587779364
Gnomad	rs587779364
Varsome	rs587779364
LitVar	rs587779364
Map	rs587779364
PheGenI	rs587779364
Biobank	rs587779364
1000 genomes	rs587779364
hgdp	rs587779364
ensembl	rs587779364
geneview	rs587779364
scholar	rs587779364
google	rs587779364
pharmgkb	rs587779364
gwascentral	rs587779364
openSNP	rs587779364
23andMe	rs587779364
SNPshot	rs587779364
SNPdbe	rs587779364
MSV3d	rs587779364
GWAS Ctlg	rs587779364

Max Magnitude

6

ClinVar
Risk	rs587779364(C;C)
Alt	rs587779364(C;C)
Reference	Rs587779364(-;-)
Significance	Pathogenic
Disease	Familial cancer of breast Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32913856dupC
CLNSRC
CLNACC	RCV000074538.3, RCV000241024.1,