rs397507947

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;A)	0	common in clinvar

Make rs397507947(-;-)

Make rs397507947(-;A)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32363177

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507947
dbSNP (classic)	rs397507947
ClinGen	rs397507947
ebi	rs397507947
HLI	rs397507947
Exac	rs397507947
Gnomad	rs397507947
Varsome	rs397507947
LitVar	rs397507947
Map	rs397507947
PheGenI	rs397507947
Biobank	rs397507947
1000 genomes	rs397507947
hgdp	rs397507947
ensembl	rs397507947
geneview	rs397507947
scholar	rs397507947
google	rs397507947
pharmgkb	rs397507947
gwascentral	rs397507947
openSNP	rs397507947
23andMe	rs397507947
SNPshot	rs397507947
SNPdbe	rs397507947
MSV3d	rs397507947
GWAS Ctlg	rs397507947

Max Magnitude

0

ClinVar
Risk	rs397507947(-;-)
Alt	rs397507947(-;-)
Reference	Rs397507947(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.32937314delA
CLNSRC	ClinVar
CLNACC	RCV000045369.2, RCV000258433.1,