rs397507967

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;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 rs397507967(G;G)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32363397

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507967
dbSNP (classic)	rs397507967
ClinGen	rs397507967
ebi	rs397507967
HLI	rs397507967
Exac	rs397507967
Gnomad	rs397507967
Varsome	rs397507967
LitVar	rs397507967
Map	rs397507967
PheGenI	rs397507967
Biobank	rs397507967
1000 genomes	rs397507967
hgdp	rs397507967
ensembl	rs397507967
geneview	rs397507967
scholar	rs397507967
google	rs397507967
pharmgkb	rs397507967
gwascentral	rs397507967
openSNP	rs397507967
23andMe	rs397507967
SNPshot	rs397507967
SNPdbe	rs397507967
MSV3d	rs397507967
GWAS Ctlg	rs397507967

Max Magnitude

6

ClinVar
Risk	rs397507967(A;A) rs397507967(G;G)
Alt	rs397507967(A;A) rs397507967(G;G)
Reference	Rs397507967(T;T)
Significance	Pathogenic
Disease	Breast-ovarian cancer Familial cancer of breast Neoplasm of breast
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2 Familial cancer of breast Neoplasm of breast
Reversed	0
HGVS	NC_000013.10:g.32937534T>A; NC_000013.10:g.32937534T>G
CLNSRC	ClinVar
CLNACC	RCV000257040.1, RCV000045450.2, RCV000257547.2, RCV000412877.1,