rs397507764

Orientation

plus

Stabilized

plus

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

Make rs397507764(A;A)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32326284

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507764
dbSNP (classic)	rs397507764
ClinGen	rs397507764
ebi	rs397507764
HLI	rs397507764
Exac	rs397507764
Gnomad	rs397507764
Varsome	rs397507764
LitVar	rs397507764
Map	rs397507764
PheGenI	rs397507764
Biobank	rs397507764
1000 genomes	rs397507764
hgdp	rs397507764
ensembl	rs397507764
geneview	rs397507764
scholar	rs397507764
google	rs397507764
pharmgkb	rs397507764
gwascentral	rs397507764
openSNP	rs397507764
23andMe	rs397507764
SNPshot	rs397507764
SNPdbe	rs397507764
MSV3d	rs397507764
GWAS Ctlg	rs397507764

Max Magnitude

6

ClinVar
Risk	rs397507764(A;A)
Alt	rs397507764(A;A)
Reference	Rs397507764(T;T)
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.32900421T>A
CLNSRC	ClinVar
CLNACC	RCV000044577.2, RCV000258414.1,