rs397507422

Orientation

plus

Stabilized

plus

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

Make rs397507422(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32380124

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507422
dbSNP (classic)	rs397507422
ClinGen	rs397507422
ebi	rs397507422
HLI	rs397507422
Exac	rs397507422
Gnomad	rs397507422
Varsome	rs397507422
LitVar	rs397507422
Map	rs397507422
PheGenI	rs397507422
Biobank	rs397507422
1000 genomes	rs397507422
hgdp	rs397507422
ensembl	rs397507422
geneview	rs397507422
scholar	rs397507422
google	rs397507422
pharmgkb	rs397507422
gwascentral	rs397507422
openSNP	rs397507422
23andMe	rs397507422
SNPshot	rs397507422
SNPdbe	rs397507422
MSV3d	rs397507422
GWAS Ctlg	rs397507422

Max Magnitude

6

ClinVar
Risk	rs397507422(-;-)
Alt	rs397507422(-;-)
Reference	Rs397507422(G;G)
Significance	Pathogenic
Disease	Breast-ovarian cancer not provided
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2 not provided
Reversed	0
HGVS	NC_000013.10:g.32954261delG
CLNSRC	ClinVar
CLNACC	RCV000031804.5, RCV000235872.1,