rs397507657

Orientation

plus

Stabilized

plus

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

Make rs397507657(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32337550

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507657
dbSNP (classic)	rs397507657
ClinGen	rs397507657
ebi	rs397507657
HLI	rs397507657
Exac	rs397507657
Gnomad	rs397507657
Varsome	rs397507657
LitVar	rs397507657
Map	rs397507657
PheGenI	rs397507657
Biobank	rs397507657
1000 genomes	rs397507657
hgdp	rs397507657
ensembl	rs397507657
geneview	rs397507657
scholar	rs397507657
google	rs397507657
pharmgkb	rs397507657
gwascentral	rs397507657
openSNP	rs397507657
23andMe	rs397507657
SNPshot	rs397507657
SNPdbe	rs397507657
MSV3d	rs397507657
GWAS Ctlg	rs397507657

Max Magnitude

6

ClinVar
Risk	rs397507657(-;-)
Alt	rs397507657(-;-)
Reference	Rs397507657(T;T)
Significance	Pathogenic
Disease	Familial cancer of breast Hereditary cancer-predisposing syndrome Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast Hereditary cancer-predisposing syndrome Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32911687delT
CLNSRC	ClinVar
CLNACC	RCV000044144.2, RCV000166884.1, RCV000241052.2,