rs397507991

Orientation

plus

Stabilized

plus

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

Make rs397507991(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32371014

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507991
dbSNP (classic)	rs397507991
ClinGen	rs397507991
ebi	rs397507991
HLI	rs397507991
Exac	rs397507991
Gnomad	rs397507991
Varsome	rs397507991
LitVar	rs397507991
Map	rs397507991
PheGenI	rs397507991
Biobank	rs397507991
1000 genomes	rs397507991
hgdp	rs397507991
ensembl	rs397507991
geneview	rs397507991
scholar	rs397507991
google	rs397507991
pharmgkb	rs397507991
gwascentral	rs397507991
openSNP	rs397507991
23andMe	rs397507991
SNPshot	rs397507991
SNPdbe	rs397507991
MSV3d	rs397507991
GWAS Ctlg	rs397507991

Max Magnitude

6

ClinVar
Risk	rs397507991(-;-)
Alt	rs397507991(-;-)
Reference	Rs397507991(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.32945151delA
CLNSRC	ClinVar
CLNACC	RCV000045553.2, RCV000256678.2,