rs397507930

Orientation

plus

Stabilized

plus

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

Make rs397507930(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32331004

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507930
dbSNP (classic)	rs397507930
ClinGen	rs397507930
ebi	rs397507930
HLI	rs397507930
Exac	rs397507930
Gnomad	rs397507930
Varsome	rs397507930
LitVar	rs397507930
Map	rs397507930
PheGenI	rs397507930
Biobank	rs397507930
1000 genomes	rs397507930
hgdp	rs397507930
ensembl	rs397507930
geneview	rs397507930
scholar	rs397507930
google	rs397507930
pharmgkb	rs397507930
gwascentral	rs397507930
openSNP	rs397507930
23andMe	rs397507930
SNPshot	rs397507930
SNPdbe	rs397507930
MSV3d	rs397507930
GWAS Ctlg	rs397507930

Max Magnitude

6

ClinVar
Risk	rs397507930(-;-)
Alt	rs397507930(-;-)
Reference	Rs397507930(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.32905141delC
CLNSRC	ClinVar
CLNACC	RCV000045283.2, RCV000225568.2,