rs397507325

Orientation

plus

Stabilized

plus

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

Make rs397507325(A;A)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32338506

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507325
dbSNP (classic)	rs397507325
ClinGen	rs397507325
ebi	rs397507325
HLI	rs397507325
Exac	rs397507325
Gnomad	rs397507325
Varsome	rs397507325
LitVar	rs397507325
Map	rs397507325
PheGenI	rs397507325
Biobank	rs397507325
1000 genomes	rs397507325
hgdp	rs397507325
ensembl	rs397507325
geneview	rs397507325
scholar	rs397507325
google	rs397507325
pharmgkb	rs397507325
gwascentral	rs397507325
openSNP	rs397507325
23andMe	rs397507325
SNPshot	rs397507325
SNPdbe	rs397507325
MSV3d	rs397507325
GWAS Ctlg	rs397507325

Max Magnitude

6

ClinVar
Risk	rs397507325(A;A)
Alt	rs397507325(A;A)
Reference	Rs397507325(T;T)
Significance	Pathogenic
Disease	Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32912643T>A
CLNSRC	ClinVar
CLNACC	RCV000031465.5,