rs397507811

Orientation

plus

Stabilized

plus

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

Make rs397507811(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32340253

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507811
dbSNP (classic)	rs397507811
ClinGen	rs397507811
ebi	rs397507811
HLI	rs397507811
Exac	rs397507811
Gnomad	rs397507811
Varsome	rs397507811
LitVar	rs397507811
Map	rs397507811
PheGenI	rs397507811
Biobank	rs397507811
1000 genomes	rs397507811
hgdp	rs397507811
ensembl	rs397507811
geneview	rs397507811
scholar	rs397507811
google	rs397507811
pharmgkb	rs397507811
gwascentral	rs397507811
openSNP	rs397507811
23andMe	rs397507811
SNPshot	rs397507811
SNPdbe	rs397507811
MSV3d	rs397507811
GWAS Ctlg	rs397507811

Max Magnitude

6

ClinVar
Risk	rs397507811(-;-)
Alt	rs397507811(-;-)
Reference	Rs397507811(T;T)
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.32914390delT
CLNSRC	ClinVar
CLNACC	RCV000044789.2, RCV000257211.2,