rs397507885

Orientation

plus

Stabilized

plus

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

Make rs397507885(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32341169

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507885
dbSNP (classic)	rs397507885
ClinGen	rs397507885
ebi	rs397507885
HLI	rs397507885
Exac	rs397507885
Gnomad	rs397507885
Varsome	rs397507885
LitVar	rs397507885
Map	rs397507885
PheGenI	rs397507885
Biobank	rs397507885
1000 genomes	rs397507885
hgdp	rs397507885
ensembl	rs397507885
geneview	rs397507885
scholar	rs397507885
google	rs397507885
pharmgkb	rs397507885
gwascentral	rs397507885
openSNP	rs397507885
23andMe	rs397507885
SNPshot	rs397507885
SNPdbe	rs397507885
MSV3d	rs397507885
GWAS Ctlg	rs397507885

Max Magnitude

6

ClinVar
Risk	rs397507885(-;-)
Alt	rs397507885(-;-)
Reference	Rs397507885(A;A)
Significance	Pathogenic
Disease	Familial cancer of breast Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32915306delA
CLNSRC	ClinVar
CLNACC	RCV000045060.2, RCV000256890.2,