rs397507592

Orientation

plus

Stabilized

plus

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

Make rs397507592(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32332992

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507592
dbSNP (classic)	rs397507592
ClinGen	rs397507592
ebi	rs397507592
HLI	rs397507592
Exac	rs397507592
Gnomad	rs397507592
Varsome	rs397507592
LitVar	rs397507592
Map	rs397507592
PheGenI	rs397507592
Biobank	rs397507592
1000 genomes	rs397507592
hgdp	rs397507592
ensembl	rs397507592
geneview	rs397507592
scholar	rs397507592
google	rs397507592
pharmgkb	rs397507592
gwascentral	rs397507592
openSNP	rs397507592
23andMe	rs397507592
SNPshot	rs397507592
SNPdbe	rs397507592
MSV3d	rs397507592
GWAS Ctlg	rs397507592

Max Magnitude

6

ClinVar
Risk	rs397507592(-;-)
Alt	rs397507592(-;-)
Reference	Rs397507592(T;T)
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.32907129delT
CLNSRC	ClinVar
CLNACC	RCV000043821.2, RCV000257416.2,