rs397508062

Orientation

plus

Stabilized

plus

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

Make rs397508062(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32396937

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397508062
dbSNP (classic)	rs397508062
ClinGen	rs397508062
ebi	rs397508062
HLI	rs397508062
Exac	rs397508062
Gnomad	rs397508062
Varsome	rs397508062
LitVar	rs397508062
Map	rs397508062
PheGenI	rs397508062
Biobank	rs397508062
1000 genomes	rs397508062
hgdp	rs397508062
ensembl	rs397508062
geneview	rs397508062
scholar	rs397508062
google	rs397508062
pharmgkb	rs397508062
gwascentral	rs397508062
openSNP	rs397508062
23andMe	rs397508062
SNPshot	rs397508062
SNPdbe	rs397508062
MSV3d	rs397508062
GWAS Ctlg	rs397508062

Max Magnitude

6

ClinVar
Risk	rs397508062(-;-)
Alt	rs397508062(-;-)
Reference	Rs397508062(ATGCATATACTGCA;ATGCATATACTGCA)
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.32971074_32971087delATGCATATACTGCA
CLNSRC	ClinVar
CLNACC	RCV000045852.2, RCV000077473.3,