rs397507716

Orientation

plus

Stabilized

plus

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

Make rs397507716(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32326113

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507716
dbSNP (classic)	rs397507716
ClinGen	rs397507716
ebi	rs397507716
HLI	rs397507716
Exac	rs397507716
Gnomad	rs397507716
Varsome	rs397507716
LitVar	rs397507716
Map	rs397507716
PheGenI	rs397507716
Biobank	rs397507716
1000 genomes	rs397507716
hgdp	rs397507716
ensembl	rs397507716
geneview	rs397507716
scholar	rs397507716
google	rs397507716
pharmgkb	rs397507716
gwascentral	rs397507716
openSNP	rs397507716
23andMe	rs397507716
SNPshot	rs397507716
SNPdbe	rs397507716
MSV3d	rs397507716
GWAS Ctlg	rs397507716

Max Magnitude

6

ClinVar
Risk	rs397507716(-;-)
Alt	rs397507716(-;-)
Reference	Rs397507716(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.32900250delA
CLNSRC	ClinVar
CLNACC	RCV000044403.2, RCV000257290.2,