rs397507796

Orientation

plus

Stabilized

plus

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

Make rs397507796(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32340020

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507796
dbSNP (classic)	rs397507796
ClinGen	rs397507796
ebi	rs397507796
HLI	rs397507796
Exac	rs397507796
Gnomad	rs397507796
Varsome	rs397507796
LitVar	rs397507796
Map	rs397507796
PheGenI	rs397507796
Biobank	rs397507796
1000 genomes	rs397507796
hgdp	rs397507796
ensembl	rs397507796
geneview	rs397507796
scholar	rs397507796
google	rs397507796
pharmgkb	rs397507796
gwascentral	rs397507796
openSNP	rs397507796
23andMe	rs397507796
SNPshot	rs397507796
SNPdbe	rs397507796
MSV3d	rs397507796
GWAS Ctlg	rs397507796

Max Magnitude

6

ClinVar
Risk	rs397507796(-;-)
Alt	rs397507796(-;-)
Reference	Rs397507796(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.32914157delA
CLNSRC	ClinVar
CLNACC	RCV000044715.2, RCV000257697.2,