rs876660026

Orientation

plus

Stabilized

plus

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

Make rs876660026(-;-)

Reference

GRCh38.p2 38.2/147

Chromosome

13

Position

32338815

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs876660026
dbSNP (classic)	rs876660026
ClinGen	rs876660026
ebi	rs876660026
HLI	rs876660026
Exac	rs876660026
Gnomad	rs876660026
Varsome	rs876660026
LitVar	rs876660026
Map	rs876660026
PheGenI	rs876660026
Biobank	rs876660026
1000 genomes	rs876660026
hgdp	rs876660026
ensembl	rs876660026
geneview	rs876660026
scholar	rs876660026
google	rs876660026
pharmgkb	rs876660026
gwascentral	rs876660026
openSNP	rs876660026
23andMe	rs876660026
SNPshot	rs876660026
SNPdbe	rs876660026
MSV3d	rs876660026
GWAS Ctlg	rs876660026

Max Magnitude

6

ClinVar
Risk	rs876660026(-;-)
Alt	rs876660026(-;-)
Reference	Rs876660026(AA;AA)
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.32912952_32912953delAA
CLNSRC
CLNACC	RCV000214586.1, RCV000257151.2,