rs397508043

Orientation

plus

Stabilized

plus

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

Make rs397508043(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32394707

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397508043
dbSNP (classic)	rs397508043
ClinGen	rs397508043
ebi	rs397508043
HLI	rs397508043
Exac	rs397508043
Gnomad	rs397508043
Varsome	rs397508043
LitVar	rs397508043
Map	rs397508043
PheGenI	rs397508043
Biobank	rs397508043
1000 genomes	rs397508043
hgdp	rs397508043
ensembl	rs397508043
geneview	rs397508043
scholar	rs397508043
google	rs397508043
pharmgkb	rs397508043
gwascentral	rs397508043
openSNP	rs397508043
23andMe	rs397508043
SNPshot	rs397508043
SNPdbe	rs397508043
MSV3d	rs397508043
GWAS Ctlg	rs397508043

Max Magnitude

6

ClinVar
Risk	rs397508043(-;-)
Alt	rs397508043(-;-)
Reference	Rs397508043(TA;TA)
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.32968844_32968845delAT
CLNSRC	ClinVar
CLNACC	RCV000045775.2, RCV000257174.2,