rs587776351

Orientation

plus

Stabilized

plus

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

Make rs587776351(A;A)

Reference

GRCh38.p2 38.2/144

Chromosome

13

Position

32370958

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs587776351
dbSNP (classic)	rs587776351
ClinGen	rs587776351
ebi	rs587776351
HLI	rs587776351
Exac	rs587776351
Gnomad	rs587776351
Varsome	rs587776351
LitVar	rs587776351
Map	rs587776351
PheGenI	rs587776351
Biobank	rs587776351
1000 genomes	rs587776351
hgdp	rs587776351
ensembl	rs587776351
geneview	rs587776351
scholar	rs587776351
google	rs587776351
pharmgkb	rs587776351
gwascentral	rs587776351
openSNP	rs587776351
23andMe	rs587776351
SNPshot	rs587776351
SNPdbe	rs587776351
MSV3d	rs587776351
GWAS Ctlg	rs587776351

Max Magnitude

6

ClinVar
Risk	rs587776351(A;A)
Alt	rs587776351(A;A)
Reference	Rs587776351(G;G)
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.32945095G>A
CLNSRC
CLNACC	RCV000143787.1, RCV000257621.2,