rs876658589

Orientation

plus

Stabilized

plus

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

Make rs876658589(-;-)

Reference

GRCh38.p2 38.2/147

Chromosome

13

Position

32332612

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs876658589
dbSNP (classic)	rs876658589
ClinGen	rs876658589
ebi	rs876658589
HLI	rs876658589
Exac	rs876658589
Gnomad	rs876658589
Varsome	rs876658589
LitVar	rs876658589
Map	rs876658589
PheGenI	rs876658589
Biobank	rs876658589
1000 genomes	rs876658589
hgdp	rs876658589
ensembl	rs876658589
geneview	rs876658589
scholar	rs876658589
google	rs876658589
pharmgkb	rs876658589
gwascentral	rs876658589
openSNP	rs876658589
23andMe	rs876658589
SNPshot	rs876658589
SNPdbe	rs876658589
MSV3d	rs876658589
GWAS Ctlg	rs876658589

Max Magnitude

6

ClinVar
Risk	rs876658589(-;-)
Alt	rs876658589(-;-)
Reference	Rs876658589(T;T)
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.32906749delT
CLNSRC
CLNACC	RCV000218138.1, RCV000256982.2,