rs397507948

Orientation

plus

Stabilized

plus

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

Make rs397507948(C;G)

Make rs397507948(G;G)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32363172

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507948
dbSNP (classic)	rs397507948
ClinGen	rs397507948
ebi	rs397507948
HLI	rs397507948
Exac	rs397507948
Gnomad	rs397507948
Varsome	rs397507948
LitVar	rs397507948
Map	rs397507948
PheGenI	rs397507948
Biobank	rs397507948
1000 genomes	rs397507948
hgdp	rs397507948
ensembl	rs397507948
geneview	rs397507948
scholar	rs397507948
google	rs397507948
pharmgkb	rs397507948
gwascentral	rs397507948
openSNP	rs397507948
23andMe	rs397507948
SNPshot	rs397507948
SNPdbe	rs397507948
MSV3d	rs397507948
GWAS Ctlg	rs397507948

Max Magnitude

0

ClinVar
Risk	rs397507948(G;G)
Alt	rs397507948(G;G)
Reference	Rs397507948(C;C)
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.32937309C>G
CLNSRC	ClinVar
CLNACC	RCV000045370.2, RCV000258340.1,