rs397507772

Orientation

plus

Stabilized

plus

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

Make rs397507772(A;A)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32316511

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507772
dbSNP (classic)	rs397507772
ClinGen	rs397507772
ebi	rs397507772
HLI	rs397507772
Exac	rs397507772
Gnomad	rs397507772
Varsome	rs397507772
LitVar	rs397507772
Map	rs397507772
PheGenI	rs397507772
Biobank	rs397507772
1000 genomes	rs397507772
hgdp	rs397507772
ensembl	rs397507772
geneview	rs397507772
scholar	rs397507772
google	rs397507772
pharmgkb	rs397507772
gwascentral	rs397507772
openSNP	rs397507772
23andMe	rs397507772
SNPshot	rs397507772
SNPdbe	rs397507772
MSV3d	rs397507772
GWAS Ctlg	rs397507772

Max Magnitude

6

ClinVar
Risk	rs397507772(A;A)
Alt	rs397507772(A;A)
Reference	Rs397507772(-;-)
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.32890648dupA
CLNSRC	ClinVar
CLNACC	RCV000044605.2, RCV000256909.2,