rs397507934

Orientation

plus

Stabilized

plus

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

Make rs397507934(A;A)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32357821

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507934
dbSNP (classic)	rs397507934
ClinGen	rs397507934
ebi	rs397507934
HLI	rs397507934
Exac	rs397507934
Gnomad	rs397507934
Varsome	rs397507934
LitVar	rs397507934
Map	rs397507934
PheGenI	rs397507934
Biobank	rs397507934
1000 genomes	rs397507934
hgdp	rs397507934
ensembl	rs397507934
geneview	rs397507934
scholar	rs397507934
google	rs397507934
pharmgkb	rs397507934
gwascentral	rs397507934
openSNP	rs397507934
23andMe	rs397507934
SNPshot	rs397507934
SNPdbe	rs397507934
MSV3d	rs397507934
GWAS Ctlg	rs397507934

Max Magnitude

6

ClinVar
Risk	rs397507934(A;A)
Alt	rs397507934(A;A)
Reference	Rs397507934(-;-)
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.32931958dupA
CLNSRC	ClinVar
CLNACC	RCV000045291.2, RCV000241396.1,