rs397507644

Orientation

plus

Stabilized

plus

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

Make rs397507644(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32337200

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507644
dbSNP (classic)	rs397507644
ClinGen	rs397507644
ebi	rs397507644
HLI	rs397507644
Exac	rs397507644
Gnomad	rs397507644
Varsome	rs397507644
LitVar	rs397507644
Map	rs397507644
PheGenI	rs397507644
Biobank	rs397507644
1000 genomes	rs397507644
hgdp	rs397507644
ensembl	rs397507644
geneview	rs397507644
scholar	rs397507644
google	rs397507644
pharmgkb	rs397507644
gwascentral	rs397507644
openSNP	rs397507644
23andMe	rs397507644
SNPshot	rs397507644
SNPdbe	rs397507644
MSV3d	rs397507644
GWAS Ctlg	rs397507644

Max Magnitude

6

ClinVar
Risk	rs397507644(-;-)
Alt	rs397507644(-;-)
Reference	Rs397507644(T;T)
Significance	Pathogenic
Disease	Familial cancer of breast Breast-ovarian cancer not provided
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast Breast-ovarian cancer, familial 2 not provided
Reversed	0
HGVS	NC_000013.10:g.32911337delT
CLNSRC	ClinVar
CLNACC	RCV000044074.2, RCV000257690.2, RCV000479662.1,