rs397507914

Orientation

plus

Stabilized

plus

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

Make rs397507914(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32355232

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507914
dbSNP (classic)	rs397507914
ClinGen	rs397507914
ebi	rs397507914
HLI	rs397507914
Exac	rs397507914
Gnomad	rs397507914
Varsome	rs397507914
LitVar	rs397507914
Map	rs397507914
PheGenI	rs397507914
Biobank	rs397507914
1000 genomes	rs397507914
hgdp	rs397507914
ensembl	rs397507914
geneview	rs397507914
scholar	rs397507914
google	rs397507914
pharmgkb	rs397507914
gwascentral	rs397507914
openSNP	rs397507914
23andMe	rs397507914
SNPshot	rs397507914
SNPdbe	rs397507914
MSV3d	rs397507914
GWAS Ctlg	rs397507914

Max Magnitude

6

ClinVar
Risk	rs397507914(-;-)
Alt	rs397507914(-;-)
Reference	Rs397507914(A;A)
Significance	Pathogenic
Disease	Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32929369delA
CLNSRC	ClinVar
CLNACC	RCV000045195.3, RCV000257436.2,