rs397507702

Orientation

plus

Stabilized

plus

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

Make rs397507702(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32338376

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507702
dbSNP (classic)	rs397507702
ClinGen	rs397507702
ebi	rs397507702
HLI	rs397507702
Exac	rs397507702
Gnomad	rs397507702
Varsome	rs397507702
LitVar	rs397507702
Map	rs397507702
PheGenI	rs397507702
Biobank	rs397507702
1000 genomes	rs397507702
hgdp	rs397507702
ensembl	rs397507702
geneview	rs397507702
scholar	rs397507702
google	rs397507702
pharmgkb	rs397507702
gwascentral	rs397507702
openSNP	rs397507702
23andMe	rs397507702
SNPshot	rs397507702
SNPdbe	rs397507702
MSV3d	rs397507702
GWAS Ctlg	rs397507702

Max Magnitude

6

ClinVar
Risk	rs397507702(-;-)
Alt	rs397507702(-;-)
Reference	Rs397507702(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.32912513delT
CLNSRC	ClinVar
CLNACC	RCV000044332.2, RCV000257014.2,