rs397508007

Orientation

plus

Stabilized

plus

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

Make rs397508007(C;C)

Make rs397508007(C;G)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32376794

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397508007
dbSNP (classic)	rs397508007
ClinGen	rs397508007
ebi	rs397508007
HLI	rs397508007
Exac	rs397508007
Gnomad	rs397508007
Varsome	rs397508007
LitVar	rs397508007
Map	rs397508007
PheGenI	rs397508007
Biobank	rs397508007
1000 genomes	rs397508007
hgdp	rs397508007
ensembl	rs397508007
geneview	rs397508007
scholar	rs397508007
google	rs397508007
pharmgkb	rs397508007
gwascentral	rs397508007
openSNP	rs397508007
23andMe	rs397508007
SNPshot	rs397508007
SNPdbe	rs397508007
MSV3d	rs397508007
GWAS Ctlg	rs397508007

Max Magnitude

0

ClinVar
Risk	rs397508007(C;C)
Alt	rs397508007(C;C)
Reference	Rs397508007(G;G)
Significance	Pathogenic
Disease	Hereditary breast and ovarian cancer syndrome Hereditary cancer-predisposing syndrome Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Hereditary breast and ovarian cancer syndrome Hereditary cancer-predisposing syndrome Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32950931G>C
CLNSRC	Ambry Genetics ClinVar
CLNACC	RCV000045614.5, RCV000131319.3, RCV000258465.1,