rs397507353

Orientation

plus

Stabilized

plus

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

Make rs397507353(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32339853

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507353
dbSNP (classic)	rs397507353
ClinGen	rs397507353
ebi	rs397507353
HLI	rs397507353
Exac	rs397507353
Gnomad	rs397507353
Varsome	rs397507353
LitVar	rs397507353
Map	rs397507353
PheGenI	rs397507353
Biobank	rs397507353
1000 genomes	rs397507353
hgdp	rs397507353
ensembl	rs397507353
geneview	rs397507353
scholar	rs397507353
google	rs397507353
pharmgkb	rs397507353
gwascentral	rs397507353
openSNP	rs397507353
23andMe	rs397507353
SNPshot	rs397507353
SNPdbe	rs397507353
MSV3d	rs397507353
GWAS Ctlg	rs397507353

Max Magnitude

6

ClinVar
Risk	rs397507353(-;-)
Alt	rs397507353(-;-)
Reference	Rs397507353(A;A)
Significance	Pathogenic
Disease	Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32913990delA
CLNSRC	ClinVar
CLNACC	RCV000031551.4,