rs397507320

Orientation

plus

Stabilized

plus

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

Make rs397507320(A;A)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32325155

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507320
dbSNP (classic)	rs397507320
ClinGen	rs397507320
ebi	rs397507320
HLI	rs397507320
Exac	rs397507320
Gnomad	rs397507320
Varsome	rs397507320
LitVar	rs397507320
Map	rs397507320
PheGenI	rs397507320
Biobank	rs397507320
1000 genomes	rs397507320
hgdp	rs397507320
ensembl	rs397507320
geneview	rs397507320
scholar	rs397507320
google	rs397507320
pharmgkb	rs397507320
gwascentral	rs397507320
openSNP	rs397507320
23andMe	rs397507320
SNPshot	rs397507320
SNPdbe	rs397507320
MSV3d	rs397507320
GWAS Ctlg	rs397507320

Max Magnitude

6

ClinVar
Risk	rs397507320(A;A)
Alt	rs397507320(A;A)
Reference	Rs397507320(T;T)
Significance	Pathogenic
Disease	Breast-ovarian cancer Familial cancer of breast
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2 Familial cancer of breast
Reversed	0
HGVS	NC_000013.10:g.32899292T>A
CLNSRC	ClinVar
CLNACC	RCV000031450.5, RCV000044326.2,