rs397507932

Orientation

plus

Stabilized

plus

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

Make rs397507932(T;T)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32357804

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507932
dbSNP (classic)	rs397507932
ClinGen	rs397507932
ebi	rs397507932
HLI	rs397507932
Exac	rs397507932
Gnomad	rs397507932
Varsome	rs397507932
LitVar	rs397507932
Map	rs397507932
PheGenI	rs397507932
Biobank	rs397507932
1000 genomes	rs397507932
hgdp	rs397507932
ensembl	rs397507932
geneview	rs397507932
scholar	rs397507932
google	rs397507932
pharmgkb	rs397507932
gwascentral	rs397507932
openSNP	rs397507932
23andMe	rs397507932
SNPshot	rs397507932
SNPdbe	rs397507932
MSV3d	rs397507932
GWAS Ctlg	rs397507932

Max Magnitude

6

ClinVar
Risk	rs397507932(T;T)
Alt	rs397507932(T;T)
Reference	Rs397507932(-;-)
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.32931941dupT
CLNSRC	ClinVar
CLNACC	RCV000045285.2, RCV000082977.4,