rs397507279

Orientation

plus

Stabilized

plus

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

Make rs397507279(A;A)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32336325

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507279
dbSNP (classic)	rs397507279
ClinGen	rs397507279
ebi	rs397507279
HLI	rs397507279
Exac	rs397507279
Gnomad	rs397507279
Varsome	rs397507279
LitVar	rs397507279
Map	rs397507279
PheGenI	rs397507279
Biobank	rs397507279
1000 genomes	rs397507279
hgdp	rs397507279
ensembl	rs397507279
geneview	rs397507279
scholar	rs397507279
google	rs397507279
pharmgkb	rs397507279
gwascentral	rs397507279
openSNP	rs397507279
23andMe	rs397507279
SNPshot	rs397507279
SNPdbe	rs397507279
MSV3d	rs397507279
GWAS Ctlg	rs397507279

Max Magnitude

6

ClinVar
Risk	rs397507279(A;A)
Alt	rs397507279(A;A)
Reference	Rs397507279(T;T)
Significance	Pathogenic
Disease	Breast-ovarian cancer Hereditary cancer-predisposing syndrome
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2 Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000013.10:g.32910462T>A
CLNSRC	ClinVar
CLNACC	RCV000031352.4, RCV000223168.1,