rs876658329

Orientation

plus

Stabilized

plus

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

Make rs876658329(-;AA)

Make rs876658329(AA;AA)

Reference

GRCh38.p2 38.2/147

Chromosome

13

Position

32338447

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs876658329
dbSNP (classic)	rs876658329
ClinGen	rs876658329
ebi	rs876658329
HLI	rs876658329
Exac	rs876658329
Gnomad	rs876658329
Varsome	rs876658329
LitVar	rs876658329
Map	rs876658329
PheGenI	rs876658329
Biobank	rs876658329
1000 genomes	rs876658329
hgdp	rs876658329
ensembl	rs876658329
geneview	rs876658329
scholar	rs876658329
google	rs876658329
pharmgkb	rs876658329
gwascentral	rs876658329
openSNP	rs876658329
23andMe	rs876658329
SNPshot	rs876658329
SNPdbe	rs876658329
MSV3d	rs876658329
GWAS Ctlg	rs876658329

Max Magnitude

6

ClinVar
Risk	rs876658329(A;A) rs876658329(AA;AA)
Alt	rs876658329(A;A) rs876658329(AA;AA)
Reference	Rs876658329(-;-)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32912584_32912585insAA; NC_000013.10:g.32912584dupA
CLNSRC
CLNACC	RCV000216793.1, RCV000465665.1, RCV000256544.2,