rs397507759

Orientation

plus

Stabilized

plus

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

Make rs397507759(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32339470

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507759
dbSNP (classic)	rs397507759
ClinGen	rs397507759
ebi	rs397507759
HLI	rs397507759
Exac	rs397507759
Gnomad	rs397507759
Varsome	rs397507759
LitVar	rs397507759
Map	rs397507759
PheGenI	rs397507759
Biobank	rs397507759
1000 genomes	rs397507759
hgdp	rs397507759
ensembl	rs397507759
geneview	rs397507759
scholar	rs397507759
google	rs397507759
pharmgkb	rs397507759
gwascentral	rs397507759
openSNP	rs397507759
23andMe	rs397507759
SNPshot	rs397507759
SNPdbe	rs397507759
MSV3d	rs397507759
GWAS Ctlg	rs397507759

Max Magnitude

6

aka c.5115_5119delAAATA

ClinVar
Risk	rs397507759(-;-)
Alt	rs397507759(-;-)
Reference	Rs397507759(AAATA;AAATA)
Significance	Untested
Disease	Familial cancer of breast
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast
Reversed	0
HGVS	NC_000013.10:g.32913607_32913611delAAATA
CLNSRC	ClinVar
CLNACC	RCV000044560.2,