rs397507632

Orientation

plus

Stabilized

plus

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

Make rs397507632(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32336944

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507632
dbSNP (classic)	rs397507632
ClinGen	rs397507632
ebi	rs397507632
HLI	rs397507632
Exac	rs397507632
Gnomad	rs397507632
Varsome	rs397507632
LitVar	rs397507632
Map	rs397507632
PheGenI	rs397507632
Biobank	rs397507632
1000 genomes	rs397507632
hgdp	rs397507632
ensembl	rs397507632
geneview	rs397507632
scholar	rs397507632
google	rs397507632
pharmgkb	rs397507632
gwascentral	rs397507632
openSNP	rs397507632
23andMe	rs397507632
SNPshot	rs397507632
SNPdbe	rs397507632
MSV3d	rs397507632
GWAS Ctlg	rs397507632

Max Magnitude

6

aka c.2589delT (p.Gln864fs)

ClinVar
Risk	rs397507632(-;-)
Alt	rs397507632(-;-)
Reference	Rs397507632(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.32911081delT
CLNSRC	ClinVar
CLNACC	RCV000044021.2, RCV000241432.1,