rs397507792

Orientation

plus

Stabilized

plus

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

Make rs397507792(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32339979

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507792
dbSNP (classic)	rs397507792
ClinGen	rs397507792
ebi	rs397507792
HLI	rs397507792
Exac	rs397507792
Gnomad	rs397507792
Varsome	rs397507792
LitVar	rs397507792
Map	rs397507792
PheGenI	rs397507792
Biobank	rs397507792
1000 genomes	rs397507792
hgdp	rs397507792
ensembl	rs397507792
geneview	rs397507792
scholar	rs397507792
google	rs397507792
pharmgkb	rs397507792
gwascentral	rs397507792
openSNP	rs397507792
23andMe	rs397507792
SNPshot	rs397507792
SNPdbe	rs397507792
MSV3d	rs397507792
GWAS Ctlg	rs397507792

Max Magnitude

6

ClinVar
Risk	rs397507792(-;-)
Alt	rs397507792(-;-)
Reference	Rs397507792(A;A)
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.32914116delA
CLNSRC	ClinVar
CLNACC	RCV000044699.2, RCV000257129.2,