rs397507977

Orientation

plus

Stabilized

plus

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

Make rs397507977(G;G)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32363529

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507977
dbSNP (classic)	rs397507977
ClinGen	rs397507977
ebi	rs397507977
HLI	rs397507977
Exac	rs397507977
Gnomad	rs397507977
Varsome	rs397507977
LitVar	rs397507977
Map	rs397507977
PheGenI	rs397507977
Biobank	rs397507977
1000 genomes	rs397507977
hgdp	rs397507977
ensembl	rs397507977
geneview	rs397507977
scholar	rs397507977
google	rs397507977
pharmgkb	rs397507977
gwascentral	rs397507977
openSNP	rs397507977
23andMe	rs397507977
SNPshot	rs397507977
SNPdbe	rs397507977
MSV3d	rs397507977
GWAS Ctlg	rs397507977

Max Magnitude

6

ClinVar
Risk	rs397507977(G;G)
Alt	rs397507977(G;G)
Reference	Rs397507977(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.32937666T>G
CLNSRC	ClinVar
CLNACC	RCV000045475.2, RCV000257530.2,