rs397508033

Orientation

plus

Stabilized

plus

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

Make rs397508033(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32332384

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397508033
dbSNP (classic)	rs397508033
ClinGen	rs397508033
ebi	rs397508033
HLI	rs397508033
Exac	rs397508033
Gnomad	rs397508033
Varsome	rs397508033
LitVar	rs397508033
Map	rs397508033
PheGenI	rs397508033
Biobank	rs397508033
1000 genomes	rs397508033
hgdp	rs397508033
ensembl	rs397508033
geneview	rs397508033
scholar	rs397508033
google	rs397508033
pharmgkb	rs397508033
gwascentral	rs397508033
openSNP	rs397508033
23andMe	rs397508033
SNPshot	rs397508033
SNPdbe	rs397508033
MSV3d	rs397508033
GWAS Ctlg	rs397508033

Max Magnitude

6

ClinVar
Risk	rs397508033(-;-)
Alt	rs397508033(-;-)
Reference	Rs397508033(C;C)
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.32906521delC
CLNSRC	ClinVar
CLNACC	RCV000045703.2, RCV000215368.1, RCV000225415.2,