rs397507884

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;A)	0	common in clinvar

Make rs397507884(A;G)

Make rs397507884(G;G)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32329496

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507884
dbSNP (classic)	rs397507884
ClinGen	rs397507884
ebi	rs397507884
HLI	rs397507884
Exac	rs397507884
Gnomad	rs397507884
Varsome	rs397507884
LitVar	rs397507884
Map	rs397507884
PheGenI	rs397507884
Biobank	rs397507884
1000 genomes	rs397507884
hgdp	rs397507884
ensembl	rs397507884
geneview	rs397507884
scholar	rs397507884
google	rs397507884
pharmgkb	rs397507884
gwascentral	rs397507884
openSNP	rs397507884
23andMe	rs397507884
SNPshot	rs397507884
SNPdbe	rs397507884
MSV3d	rs397507884
GWAS Ctlg	rs397507884

Max Magnitude

0

ClinVar
Risk	rs397507884(G;G) rs397507884(T;T)
Alt	rs397507884(G;G) rs397507884(T;T)
Reference	Rs397507884(A;A)
Significance	Pathogenic
Disease	Familial cancer of breast Breast-ovarian cancer Hereditary cancer-predisposing syndrome
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast Breast-ovarian cancer, familial 2 Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000013.10:g.32903633A>G; NC_000013.10:g.32903633A>T
CLNSRC	ClinVar
CLNACC	RCV000045057.2, RCV000258477.1, RCV000222207.1,