rs397507340

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 rs397507340(A;A)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32326241

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507340
dbSNP (classic)	rs397507340
ClinGen	rs397507340
ebi	rs397507340
HLI	rs397507340
Exac	rs397507340
Gnomad	rs397507340
Varsome	rs397507340
LitVar	rs397507340
Map	rs397507340
PheGenI	rs397507340
Biobank	rs397507340
1000 genomes	rs397507340
hgdp	rs397507340
ensembl	rs397507340
geneview	rs397507340
scholar	rs397507340
google	rs397507340
pharmgkb	rs397507340
gwascentral	rs397507340
openSNP	rs397507340
23andMe	rs397507340
SNPshot	rs397507340
SNPdbe	rs397507340
MSV3d	rs397507340
GWAS Ctlg	rs397507340

Max Magnitude

6

ClinVar
Risk	rs397507340(A;A)
Alt	rs397507340(A;A)
Reference	Rs397507340(G;G)
Significance	Pathogenic
Disease	Breast-ovarian cancer Familial cancer of breast
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2 Familial cancer of breast
Reversed	0
HGVS	NC_000013.10:g.32900378G>A
CLNSRC	ClinVar
CLNACC	RCV000031503.3, RCV000044487.2,