rs397507886

Orientation

plus

Stabilized

plus

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

Make rs397507886(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32341171

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507886
dbSNP (classic)	rs397507886
ClinGen	rs397507886
ebi	rs397507886
HLI	rs397507886
Exac	rs397507886
Gnomad	rs397507886
Varsome	rs397507886
LitVar	rs397507886
Map	rs397507886
PheGenI	rs397507886
Biobank	rs397507886
1000 genomes	rs397507886
hgdp	rs397507886
ensembl	rs397507886
geneview	rs397507886
scholar	rs397507886
google	rs397507886
pharmgkb	rs397507886
gwascentral	rs397507886
openSNP	rs397507886
23andMe	rs397507886
SNPshot	rs397507886
SNPdbe	rs397507886
MSV3d	rs397507886
GWAS Ctlg	rs397507886

Max Magnitude

6

ClinVar
Risk	rs397507886(-;-)
Alt	rs397507886(-;-)
Reference	Rs397507886(AA;AA)
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.32915308_32915309delAA
CLNSRC	ClinVar
CLNACC	RCV000045061.2, RCV000241125.2,