rs769152395

Orientation

plus

Stabilized

plus

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

Make rs769152395(G;G)

Reference

GRCh38.p2 38.2/144

Chromosome

13

Position

32319075

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs769152395
dbSNP (classic)	rs769152395
ClinGen	rs769152395
ebi	rs769152395
HLI	rs769152395
Exac	rs769152395
Gnomad	rs769152395
Varsome	rs769152395
LitVar	rs769152395
Map	rs769152395
PheGenI	rs769152395
Biobank	rs769152395
1000 genomes	rs769152395
hgdp	rs769152395
ensembl	rs769152395
geneview	rs769152395
scholar	rs769152395
google	rs769152395
pharmgkb	rs769152395
gwascentral	rs769152395
openSNP	rs769152395
23andMe	rs769152395
SNPshot	rs769152395
SNPdbe	rs769152395
MSV3d	rs769152395
GWAS Ctlg	rs769152395

Max Magnitude

6

ClinVar
Risk	rs769152395(G;G)
Alt	rs769152395(G;G)
Reference	Rs769152395(A;A)
Significance	Probable-Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	BRCA2
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000013.10:g.32893212A>G
CLNSRC
CLNACC	RCV000167275.1,