rs876658648

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar
(G;T)	6	Likely miscall in Ancestry v2c data; otherwise, BRCA2 variant considered pathogenic for breast cancer

Make rs876658648(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

13

Position

32336996

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs876658648
dbSNP (classic)	rs876658648
ClinGen	rs876658648
ebi	rs876658648
HLI	rs876658648
Exac	rs876658648
Gnomad	rs876658648
Varsome	rs876658648
LitVar	rs876658648
Map	rs876658648
PheGenI	rs876658648
Biobank	rs876658648
1000 genomes	rs876658648
hgdp	rs876658648
ensembl	rs876658648
geneview	rs876658648
scholar	rs876658648
google	rs876658648
pharmgkb	rs876658648
gwascentral	rs876658648
openSNP	rs876658648
23andMe	rs876658648
SNPshot	rs876658648
SNPdbe	rs876658648
MSV3d	rs876658648
GWAS Ctlg	rs876658648

Max Magnitude

6

ClinVar
Risk	rs876658648(T;T)
Alt	rs876658648(T;T)
Reference	Rs876658648(G;G)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Hereditary cancer-predisposing syndrome Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32911133G>T
CLNSRC
CLNACC	RCV000213781.1, RCV000256675.2,