rs876661242

Orientation

plus

Stabilized

plus

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

Make rs876661242(A;A)

Reference

GRCh38.p2 38.2/147

Chromosome

13

Position

32394813

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs876661242
dbSNP (classic)	rs876661242
ClinGen	rs876661242
ebi	rs876661242
HLI	rs876661242
Exac	rs876661242
Gnomad	rs876661242
Varsome	rs876661242
LitVar	rs876661242
Map	rs876661242
PheGenI	rs876661242
Biobank	rs876661242
1000 genomes	rs876661242
hgdp	rs876661242
ensembl	rs876661242
geneview	rs876661242
scholar	rs876661242
google	rs876661242
pharmgkb	rs876661242
gwascentral	rs876661242
openSNP	rs876661242
23andMe	rs876661242
SNPshot	rs876661242
SNPdbe	rs876661242
MSV3d	rs876661242
GWAS Ctlg	rs876661242

Max Magnitude

6

ClinVar
Risk	rs876661242(A;A)
Alt	rs876661242(A;A)
Reference	Rs876661242(G;G)
Significance	Pathogenic
Disease	not provided Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	not provided Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32968950G>A
CLNSRC
CLNACC	RCV000219823.1, RCV000229281.1, RCV000256847.2,