rs397508039

Orientation

plus

Stabilized

plus

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

Make rs397508039(T;T)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32332396

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397508039
dbSNP (classic)	rs397508039
ClinGen	rs397508039
ebi	rs397508039
HLI	rs397508039
Exac	rs397508039
Gnomad	rs397508039
Varsome	rs397508039
LitVar	rs397508039
Map	rs397508039
PheGenI	rs397508039
Biobank	rs397508039
1000 genomes	rs397508039
hgdp	rs397508039
ensembl	rs397508039
geneview	rs397508039
scholar	rs397508039
google	rs397508039
pharmgkb	rs397508039
gwascentral	rs397508039
openSNP	rs397508039
23andMe	rs397508039
SNPshot	rs397508039
SNPdbe	rs397508039
MSV3d	rs397508039
GWAS Ctlg	rs397508039

Max Magnitude

6

ClinVar
Risk	rs397508039(T;T)
Alt	rs397508039(T;T)
Reference	Rs397508039(-;-)
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.32906533dupT
CLNSRC	ClinVar
CLNACC	RCV000045741.2, RCV000256556.2,