rs397507953

Orientation

plus

Stabilized

plus

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

Make rs397507953(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32363223

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507953
dbSNP (classic)	rs397507953
ClinGen	rs397507953
ebi	rs397507953
HLI	rs397507953
Exac	rs397507953
Gnomad	rs397507953
Varsome	rs397507953
LitVar	rs397507953
Map	rs397507953
PheGenI	rs397507953
Biobank	rs397507953
1000 genomes	rs397507953
hgdp	rs397507953
ensembl	rs397507953
geneview	rs397507953
scholar	rs397507953
google	rs397507953
pharmgkb	rs397507953
gwascentral	rs397507953
openSNP	rs397507953
23andMe	rs397507953
SNPshot	rs397507953
SNPdbe	rs397507953
MSV3d	rs397507953
GWAS Ctlg	rs397507953

Max Magnitude

6

ClinVar
Risk	rs397507953(-;-)
Alt	rs397507953(-;-)
Reference	Rs397507953(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.32937360delA
CLNSRC	ClinVar
CLNACC	RCV000045389.2, RCV000238781.2,