rs397507290

Orientation

plus

Stabilized

plus

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

Make rs397507290(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32336973

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507290
dbSNP (classic)	rs397507290
ClinGen	rs397507290
ebi	rs397507290
HLI	rs397507290
Exac	rs397507290
Gnomad	rs397507290
Varsome	rs397507290
LitVar	rs397507290
Map	rs397507290
PheGenI	rs397507290
Biobank	rs397507290
1000 genomes	rs397507290
hgdp	rs397507290
ensembl	rs397507290
geneview	rs397507290
scholar	rs397507290
google	rs397507290
pharmgkb	rs397507290
gwascentral	rs397507290
openSNP	rs397507290
23andMe	rs397507290
SNPshot	rs397507290
SNPdbe	rs397507290
MSV3d	rs397507290
GWAS Ctlg	rs397507290

Max Magnitude

6

ClinVar
Risk	rs397507290(-;-)
Alt	rs397507290(-;-)
Reference	Rs397507290(AT;AT)
Significance	Pathogenic
Disease	Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32911110_32911111delTA
CLNSRC	ClinVar
CLNACC	RCV000031376.4,