rs876658631

Orientation

plus

Stabilized

plus

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

Make rs876658631(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

13

Position

32356508

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs876658631
dbSNP (classic)	rs876658631
ClinGen	rs876658631
ebi	rs876658631
HLI	rs876658631
Exac	rs876658631
Gnomad	rs876658631
Varsome	rs876658631
LitVar	rs876658631
Map	rs876658631
PheGenI	rs876658631
Biobank	rs876658631
1000 genomes	rs876658631
hgdp	rs876658631
ensembl	rs876658631
geneview	rs876658631
scholar	rs876658631
google	rs876658631
pharmgkb	rs876658631
gwascentral	rs876658631
openSNP	rs876658631
23andMe	rs876658631
SNPshot	rs876658631
SNPdbe	rs876658631
MSV3d	rs876658631
GWAS Ctlg	rs876658631

Max Magnitude

6

ClinVar
Risk	rs876658631(T;T)
Alt	rs876658631(T;T)
Reference	Rs876658631(C;C)
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.32930645C>T
CLNSRC
CLNACC	RCV000215458.1, RCV000256919.2,