rs397507891

Orientation

plus

Stabilized

plus

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

Make rs397507891(C;C)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32346897

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507891
dbSNP (classic)	rs397507891
ClinGen	rs397507891
ebi	rs397507891
HLI	rs397507891
Exac	rs397507891
Gnomad	rs397507891
Varsome	rs397507891
LitVar	rs397507891
Map	rs397507891
PheGenI	rs397507891
Biobank	rs397507891
1000 genomes	rs397507891
hgdp	rs397507891
ensembl	rs397507891
geneview	rs397507891
scholar	rs397507891
google	rs397507891
pharmgkb	rs397507891
gwascentral	rs397507891
openSNP	rs397507891
23andMe	rs397507891
SNPshot	rs397507891
SNPdbe	rs397507891
MSV3d	rs397507891
GWAS Ctlg	rs397507891

Max Magnitude

6

ClinVar
Risk	rs397507891(A;A) rs397507891(C;C) rs397507891(T;T)
Alt	rs397507891(A;A) rs397507891(C;C) rs397507891(T;T)
Reference	Rs397507891(G;G)
Significance	Pathogenic
Disease	Hereditary breast and ovarian cancer syndrome Familial cancer of breast Breast-ovarian cancer not provided
Variation	info
Gene	BRCA2
CLNDBN	Hereditary breast and ovarian cancer syndrome Familial cancer of breast Breast-ovarian cancer, familial 2 not provided
Reversed	0
HGVS	NC_000013.10:g.32921034G>A; NC_000013.10:g.32921034G>C; NC_000013.10:g.32921034G>T
CLNSRC	ClinVar
CLNACC	RCV000232637.1, RCV000045108.2, RCV000258405.1, RCV000045109.2, RCV000482364.1,