rs397507896

Orientation

plus

Stabilized

plus

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

Make rs397507896(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32354945

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507896
dbSNP (classic)	rs397507896
ClinGen	rs397507896
ebi	rs397507896
HLI	rs397507896
Exac	rs397507896
Gnomad	rs397507896
Varsome	rs397507896
LitVar	rs397507896
Map	rs397507896
PheGenI	rs397507896
Biobank	rs397507896
1000 genomes	rs397507896
hgdp	rs397507896
ensembl	rs397507896
geneview	rs397507896
scholar	rs397507896
google	rs397507896
pharmgkb	rs397507896
gwascentral	rs397507896
openSNP	rs397507896
23andMe	rs397507896
SNPshot	rs397507896
SNPdbe	rs397507896
MSV3d	rs397507896
GWAS Ctlg	rs397507896

Max Magnitude

6

ClinVar
Risk	rs397507896(-;-)
Alt	rs397507896(-;-)
Reference	Rs397507896(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.32929082delA
CLNSRC	ClinVar
CLNACC	RCV000045141.2, RCV000241029.2,