rs397507712

Orientation

plus

Stabilized

plus

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

Make rs397507712(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32338578

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507712
dbSNP (classic)	rs397507712
ClinGen	rs397507712
ebi	rs397507712
HLI	rs397507712
Exac	rs397507712
Gnomad	rs397507712
Varsome	rs397507712
LitVar	rs397507712
Map	rs397507712
PheGenI	rs397507712
Biobank	rs397507712
1000 genomes	rs397507712
hgdp	rs397507712
ensembl	rs397507712
geneview	rs397507712
scholar	rs397507712
google	rs397507712
pharmgkb	rs397507712
gwascentral	rs397507712
openSNP	rs397507712
23andMe	rs397507712
SNPshot	rs397507712
SNPdbe	rs397507712
MSV3d	rs397507712
GWAS Ctlg	rs397507712

Max Magnitude

6

ClinVar
Risk	rs397507712(-;-)
Alt	rs397507712(-;-)
Reference	Rs397507712(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.32912715delA
CLNSRC	ClinVar
CLNACC	RCV000044374.2, RCV000257844.2,