rs397507734

Orientation

plus

Stabilized

plus

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

Make rs397507734(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32339002

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507734
dbSNP (classic)	rs397507734
ClinGen	rs397507734
ebi	rs397507734
HLI	rs397507734
Exac	rs397507734
Gnomad	rs397507734
Varsome	rs397507734
LitVar	rs397507734
Map	rs397507734
PheGenI	rs397507734
Biobank	rs397507734
1000 genomes	rs397507734
hgdp	rs397507734
ensembl	rs397507734
geneview	rs397507734
scholar	rs397507734
google	rs397507734
pharmgkb	rs397507734
gwascentral	rs397507734
openSNP	rs397507734
23andMe	rs397507734
SNPshot	rs397507734
SNPdbe	rs397507734
MSV3d	rs397507734
GWAS Ctlg	rs397507734

Max Magnitude

6

ClinVar
Risk	rs397507734(-;-)
Alt	rs397507734(-;-)
Reference	Rs397507734(AGAG;AGAG)
Significance	Pathogenic
Disease	Familial cancer of breast Hereditary cancer-predisposing syndrome Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast Hereditary cancer-predisposing syndrome Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32913139_32913142delAGAG
CLNSRC	ClinVar
CLNACC	RCV000044459.2, RCV000165672.2, RCV000238961.3,