rs397507799

Orientation

plus

Stabilized

plus

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

Make rs397507799(CT;CT)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32326554

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507799
dbSNP (classic)	rs397507799
ClinGen	rs397507799
ebi	rs397507799
HLI	rs397507799
Exac	rs397507799
Gnomad	rs397507799
Varsome	rs397507799
LitVar	rs397507799
Map	rs397507799
PheGenI	rs397507799
Biobank	rs397507799
1000 genomes	rs397507799
hgdp	rs397507799
ensembl	rs397507799
geneview	rs397507799
scholar	rs397507799
google	rs397507799
pharmgkb	rs397507799
gwascentral	rs397507799
openSNP	rs397507799
23andMe	rs397507799
SNPshot	rs397507799
SNPdbe	rs397507799
MSV3d	rs397507799
GWAS Ctlg	rs397507799

Max Magnitude

6

ClinVar
Risk	rs397507799(CT;CT)
Alt	rs397507799(CT;CT)
Reference	Rs397507799(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.32900691delAinsCT
CLNSRC	ClinVar
CLNACC	RCV000044736.2, RCV000241205.2,