rs397507593

Orientation

plus

Stabilized

plus

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

Make rs397507593(G;G)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32333018

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507593
dbSNP (classic)	rs397507593
ClinGen	rs397507593
ebi	rs397507593
HLI	rs397507593
Exac	rs397507593
Gnomad	rs397507593
Varsome	rs397507593
LitVar	rs397507593
Map	rs397507593
PheGenI	rs397507593
Biobank	rs397507593
1000 genomes	rs397507593
hgdp	rs397507593
ensembl	rs397507593
geneview	rs397507593
scholar	rs397507593
google	rs397507593
pharmgkb	rs397507593
gwascentral	rs397507593
openSNP	rs397507593
23andMe	rs397507593
SNPshot	rs397507593
SNPdbe	rs397507593
MSV3d	rs397507593
GWAS Ctlg	rs397507593

Max Magnitude

6

ClinVar
Risk	rs397507593(G;G)
Alt	rs397507593(G;G)
Reference	Rs397507593(-;-)
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.32907155dupG
CLNSRC	ClinVar
CLNACC	RCV000043824.2, RCV000257403.2,