rs869320799

Orientation

plus

Stabilized

plus

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

Make rs869320799(-;-)

Reference

GRCh38.p2 38.2/147

Chromosome

13

Position

32379492

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs869320799
dbSNP (classic)	rs869320799
ClinGen	rs869320799
ebi	rs869320799
HLI	rs869320799
Exac	rs869320799
Gnomad	rs869320799
Varsome	rs869320799
LitVar	rs869320799
Map	rs869320799
PheGenI	rs869320799
Biobank	rs869320799
1000 genomes	rs869320799
hgdp	rs869320799
ensembl	rs869320799
geneview	rs869320799
scholar	rs869320799
google	rs869320799
pharmgkb	rs869320799
gwascentral	rs869320799
openSNP	rs869320799
23andMe	rs869320799
SNPshot	rs869320799
SNPdbe	rs869320799
MSV3d	rs869320799
GWAS Ctlg	rs869320799

Max Magnitude

6

ClinVar
Risk	rs869320799(-;-)
Alt	rs869320799(-;-)
Reference	Rs869320799(A;A)
Significance	Pathogenic
Disease	Breast-ovarian cancer Familial cancer of breast
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2 Familial cancer of breast
Reversed	0
HGVS	NC_000013.10:g.32953629delA
CLNSRC
CLNACC	RCV000211026.2, RCV000239309.1,