rs397507651

Orientation

plus

Stabilized

plus

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

Make rs397507651(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32337373

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507651
dbSNP (classic)	rs397507651
ClinGen	rs397507651
ebi	rs397507651
HLI	rs397507651
Exac	rs397507651
Gnomad	rs397507651
Varsome	rs397507651
LitVar	rs397507651
Map	rs397507651
PheGenI	rs397507651
Biobank	rs397507651
1000 genomes	rs397507651
hgdp	rs397507651
ensembl	rs397507651
geneview	rs397507651
scholar	rs397507651
google	rs397507651
pharmgkb	rs397507651
gwascentral	rs397507651
openSNP	rs397507651
23andMe	rs397507651
SNPshot	rs397507651
SNPdbe	rs397507651
MSV3d	rs397507651
GWAS Ctlg	rs397507651

Max Magnitude

6

ClinVar
Risk	rs397507651(-;-)
Alt	rs397507651(-;-)
Reference	Rs397507651(A;A)
Significance	Pathogenic
Disease	Familial cancer of breast Hereditary cancer-predisposing syndrome Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast Hereditary cancer-predisposing syndrome Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32911510delA
CLNSRC	ClinVar
CLNACC	RCV000044104.2, RCV000221234.1, RCV000257393.2,