rs397508054

Orientation

plus

Stabilized

plus

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

Make rs397508054(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32394906

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397508054
dbSNP (classic)	rs397508054
ClinGen	rs397508054
ebi	rs397508054
HLI	rs397508054
Exac	rs397508054
Gnomad	rs397508054
Varsome	rs397508054
LitVar	rs397508054
Map	rs397508054
PheGenI	rs397508054
Biobank	rs397508054
1000 genomes	rs397508054
hgdp	rs397508054
ensembl	rs397508054
geneview	rs397508054
scholar	rs397508054
google	rs397508054
pharmgkb	rs397508054
gwascentral	rs397508054
openSNP	rs397508054
23andMe	rs397508054
SNPshot	rs397508054
SNPdbe	rs397508054
MSV3d	rs397508054
GWAS Ctlg	rs397508054

Max Magnitude

6

ClinVar
Risk	rs397508054(-;-)
Alt	rs397508054(-;-)
Reference	Rs397508054(A;A)
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.32969043delA
CLNSRC	ClinVar
CLNACC	RCV000045830.2, RCV000257243.2,