rs786202461

Orientation

plus

Stabilized

plus

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

Make rs786202461(A;A)

Reference

GRCh38.p2 38.2/146

Chromosome

13

Position

32340510

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs786202461
dbSNP (classic)	rs786202461
ClinGen	rs786202461
ebi	rs786202461
HLI	rs786202461
Exac	rs786202461
Gnomad	rs786202461
Varsome	rs786202461
LitVar	rs786202461
Map	rs786202461
PheGenI	rs786202461
Biobank	rs786202461
1000 genomes	rs786202461
hgdp	rs786202461
ensembl	rs786202461
geneview	rs786202461
scholar	rs786202461
google	rs786202461
pharmgkb	rs786202461
gwascentral	rs786202461
openSNP	rs786202461
23andMe	rs786202461
SNPshot	rs786202461
SNPdbe	rs786202461
MSV3d	rs786202461
GWAS Ctlg	rs786202461

Max Magnitude

6

ClinVar
Risk	rs786202461(A;A) rs786202461(G;G)
Alt	rs786202461(A;A) rs786202461(G;G)
Reference	Rs786202461(C;C)
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.32914647C>A; NC_000013.10:g.32914647C>G
CLNSRC
CLNACC	RCV000165281.2, RCV000241265.1, RCV000257714.1,