rs397507827

Orientation

plus

Stabilized

plus

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

Make rs397507827(T;T)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32340437

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507827
dbSNP (classic)	rs397507827
ClinGen	rs397507827
ebi	rs397507827
HLI	rs397507827
Exac	rs397507827
Gnomad	rs397507827
Varsome	rs397507827
LitVar	rs397507827
Map	rs397507827
PheGenI	rs397507827
Biobank	rs397507827
1000 genomes	rs397507827
hgdp	rs397507827
ensembl	rs397507827
geneview	rs397507827
scholar	rs397507827
google	rs397507827
pharmgkb	rs397507827
gwascentral	rs397507827
openSNP	rs397507827
23andMe	rs397507827
SNPshot	rs397507827
SNPdbe	rs397507827
MSV3d	rs397507827
GWAS Ctlg	rs397507827

Max Magnitude

6

ClinVar
Risk	rs397507827(T;T)
Alt	rs397507827(T;T)
Reference	Rs397507827(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.32914574G>T
CLNSRC	ClinVar
CLNACC	RCV000044838.2, RCV000256860.2,