rs397507880

Orientation

plus

Stabilized

plus

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

Make rs397507880(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32329484

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507880
dbSNP (classic)	rs397507880
ClinGen	rs397507880
ebi	rs397507880
HLI	rs397507880
Exac	rs397507880
Gnomad	rs397507880
Varsome	rs397507880
LitVar	rs397507880
Map	rs397507880
PheGenI	rs397507880
Biobank	rs397507880
1000 genomes	rs397507880
hgdp	rs397507880
ensembl	rs397507880
geneview	rs397507880
scholar	rs397507880
google	rs397507880
pharmgkb	rs397507880
gwascentral	rs397507880
openSNP	rs397507880
23andMe	rs397507880
SNPshot	rs397507880
SNPdbe	rs397507880
MSV3d	rs397507880
GWAS Ctlg	rs397507880

Max Magnitude

6

ClinVar
Risk	rs397507880(-;-)
Alt	rs397507880(-;-)
Reference	Rs397507880(ACTA;ACTA)
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.32903621_32903624delACTA
CLNSRC	ClinVar
CLNACC	RCV000045036.2, RCV000257710.2,