rs397507782

Orientation

plus

Stabilized

plus

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

Make rs397507782(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32339735

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507782
dbSNP (classic)	rs397507782
ClinGen	rs397507782
ebi	rs397507782
HLI	rs397507782
Exac	rs397507782
Gnomad	rs397507782
Varsome	rs397507782
LitVar	rs397507782
Map	rs397507782
PheGenI	rs397507782
Biobank	rs397507782
1000 genomes	rs397507782
hgdp	rs397507782
ensembl	rs397507782
geneview	rs397507782
scholar	rs397507782
google	rs397507782
pharmgkb	rs397507782
gwascentral	rs397507782
openSNP	rs397507782
23andMe	rs397507782
SNPshot	rs397507782
SNPdbe	rs397507782
MSV3d	rs397507782
GWAS Ctlg	rs397507782

Max Magnitude

6

ClinVar
Risk	rs397507782(-;-)
Alt	rs397507782(-;-)
Reference	Rs397507782(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.32913872delG
CLNSRC	ClinVar
CLNACC	RCV000044645.2, RCV000257237.1,