rs879255458

Orientation

plus

Stabilized

plus

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

Make rs879255458(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

13

Position

32339648

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs879255458
dbSNP (classic)	rs879255458
ClinGen	rs879255458
ebi	rs879255458
HLI	rs879255458
Exac	rs879255458
Gnomad	rs879255458
Varsome	rs879255458
LitVar	rs879255458
Map	rs879255458
PheGenI	rs879255458
Biobank	rs879255458
1000 genomes	rs879255458
hgdp	rs879255458
ensembl	rs879255458
geneview	rs879255458
scholar	rs879255458
google	rs879255458
pharmgkb	rs879255458
gwascentral	rs879255458
openSNP	rs879255458
23andMe	rs879255458
SNPshot	rs879255458
SNPdbe	rs879255458
MSV3d	rs879255458
GWAS Ctlg	rs879255458

Max Magnitude

6

ClinVar
Risk	rs879255458(T;T)
Alt	rs879255458(T;T)
Reference	Rs879255458(A;A)
Significance	Pathogenic
Disease	Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32913785A>T
CLNSRC
CLNACC	RCV000238810.1,