rs397507800

Orientation

plus

Stabilized

plus

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

Make rs397507800(T;T)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32340089

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507800
dbSNP (classic)	rs397507800
ClinGen	rs397507800
ebi	rs397507800
HLI	rs397507800
Exac	rs397507800
Gnomad	rs397507800
Varsome	rs397507800
LitVar	rs397507800
Map	rs397507800
PheGenI	rs397507800
Biobank	rs397507800
1000 genomes	rs397507800
hgdp	rs397507800
ensembl	rs397507800
geneview	rs397507800
scholar	rs397507800
google	rs397507800
pharmgkb	rs397507800
gwascentral	rs397507800
openSNP	rs397507800
23andMe	rs397507800
SNPshot	rs397507800
SNPdbe	rs397507800
MSV3d	rs397507800
GWAS Ctlg	rs397507800

Max Magnitude

6

ClinVar
Risk	rs397507800(T;T)
Alt	rs397507800(T;T)
Reference	Rs397507800(G;G)
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.32914226G>T
CLNSRC	ClinVar
CLNACC	RCV000044737.2, RCV000257767.2,