rs397507628

Orientation

plus

Stabilized

plus

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

Make rs397507628(T;T)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32319253

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507628
dbSNP (classic)	rs397507628
ClinGen	rs397507628
ebi	rs397507628
HLI	rs397507628
Exac	rs397507628
Gnomad	rs397507628
Varsome	rs397507628
LitVar	rs397507628
Map	rs397507628
PheGenI	rs397507628
Biobank	rs397507628
1000 genomes	rs397507628
hgdp	rs397507628
ensembl	rs397507628
geneview	rs397507628
scholar	rs397507628
google	rs397507628
pharmgkb	rs397507628
gwascentral	rs397507628
openSNP	rs397507628
23andMe	rs397507628
SNPshot	rs397507628
SNPdbe	rs397507628
MSV3d	rs397507628
GWAS Ctlg	rs397507628

Max Magnitude

6

ClinVar
Risk	rs397507628(C;C) rs397507628(T;T)
Alt	rs397507628(C;C) rs397507628(T;T)
Reference	Rs397507628(A;A)
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.32893390A>T
CLNSRC	ClinVar
CLNACC	RCV000043997.2, RCV000257796.2,