rs397507839

Orientation

plus

Stabilized

plus

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

Make rs397507839(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32340657

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507839
dbSNP (classic)	rs397507839
ClinGen	rs397507839
ebi	rs397507839
HLI	rs397507839
Exac	rs397507839
Gnomad	rs397507839
Varsome	rs397507839
LitVar	rs397507839
Map	rs397507839
PheGenI	rs397507839
Biobank	rs397507839
1000 genomes	rs397507839
hgdp	rs397507839
ensembl	rs397507839
geneview	rs397507839
scholar	rs397507839
google	rs397507839
pharmgkb	rs397507839
gwascentral	rs397507839
openSNP	rs397507839
23andMe	rs397507839
SNPshot	rs397507839
SNPdbe	rs397507839
MSV3d	rs397507839
GWAS Ctlg	rs397507839

Max Magnitude

6

ClinVar
Risk	rs397507839(-;-)
Alt	rs397507839(-;-)
Reference	Rs397507839(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.32914794delA
CLNSRC	ClinVar
CLNACC	RCV000044892.2, RCV000257485.2,