rs397508058

Orientation

plus

Stabilized

plus

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

Make rs397508058(A;A)

Make rs397508058(A;G)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32394934

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397508058
dbSNP (classic)	rs397508058
ClinGen	rs397508058
ebi	rs397508058
HLI	rs397508058
Exac	rs397508058
Gnomad	rs397508058
Varsome	rs397508058
LitVar	rs397508058
Map	rs397508058
PheGenI	rs397508058
Biobank	rs397508058
1000 genomes	rs397508058
hgdp	rs397508058
ensembl	rs397508058
geneview	rs397508058
scholar	rs397508058
google	rs397508058
pharmgkb	rs397508058
gwascentral	rs397508058
openSNP	rs397508058
23andMe	rs397508058
SNPshot	rs397508058
SNPdbe	rs397508058
MSV3d	rs397508058
GWAS Ctlg	rs397508058

Max Magnitude

0

ClinVar
Risk	rs397508058(A;A) rs397508058(T;T)
Alt	rs397508058(A;A) rs397508058(T;T)
Reference	Rs397508058(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.32969071G>A; NC_000013.10:g.32969071G>T
CLNSRC	ClinVar
CLNACC	RCV000045837.2, RCV000258387.1, RCV000258166.1,