rs397507718

Orientation

plus

Stabilized

plus

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

Make rs397507718(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32338764

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507718
dbSNP (classic)	rs397507718
ClinGen	rs397507718
ebi	rs397507718
HLI	rs397507718
Exac	rs397507718
Gnomad	rs397507718
Varsome	rs397507718
LitVar	rs397507718
Map	rs397507718
PheGenI	rs397507718
Biobank	rs397507718
1000 genomes	rs397507718
hgdp	rs397507718
ensembl	rs397507718
geneview	rs397507718
scholar	rs397507718
google	rs397507718
pharmgkb	rs397507718
gwascentral	rs397507718
openSNP	rs397507718
23andMe	rs397507718
SNPshot	rs397507718
SNPdbe	rs397507718
MSV3d	rs397507718
GWAS Ctlg	rs397507718

Max Magnitude

6

ClinVar
Risk	rs397507718(-;-)
Alt	rs397507718(-;-)
Reference	Rs397507718(ATAAG;ATAAG)
Significance	Pathogenic
Disease	Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32912901_32912905delTAAGA
CLNSRC	ClinVar
CLNACC	RCV000044407.3, RCV000238723.3,