rs397507752

Orientation

plus

Stabilized

plus

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

Make rs397507752(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32339307

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507752
dbSNP (classic)	rs397507752
ClinGen	rs397507752
ebi	rs397507752
HLI	rs397507752
Exac	rs397507752
Gnomad	rs397507752
Varsome	rs397507752
LitVar	rs397507752
Map	rs397507752
PheGenI	rs397507752
Biobank	rs397507752
1000 genomes	rs397507752
hgdp	rs397507752
ensembl	rs397507752
geneview	rs397507752
scholar	rs397507752
google	rs397507752
pharmgkb	rs397507752
gwascentral	rs397507752
openSNP	rs397507752
23andMe	rs397507752
SNPshot	rs397507752
SNPdbe	rs397507752
MSV3d	rs397507752
GWAS Ctlg	rs397507752

Max Magnitude

6

ClinVar
Risk	rs397507752(-;-)
Alt	rs397507752(-;-)
Reference	Rs397507752(C;C)
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.32913444delC
CLNSRC	ClinVar
CLNACC	RCV000044530.2, RCV000257364.2,