rs869320783

Orientation

plus

Stabilized

plus

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

Make rs869320783(-;-)

Reference

GRCh38.p2 38.2/147

Chromosome

13

Position

32338970

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs869320783
dbSNP (classic)	rs869320783
ClinGen	rs869320783
ebi	rs869320783
HLI	rs869320783
Exac	rs869320783
Gnomad	rs869320783
Varsome	rs869320783
LitVar	rs869320783
Map	rs869320783
PheGenI	rs869320783
Biobank	rs869320783
1000 genomes	rs869320783
hgdp	rs869320783
ensembl	rs869320783
geneview	rs869320783
scholar	rs869320783
google	rs869320783
pharmgkb	rs869320783
gwascentral	rs869320783
openSNP	rs869320783
23andMe	rs869320783
SNPshot	rs869320783
SNPdbe	rs869320783
MSV3d	rs869320783
GWAS Ctlg	rs869320783

Max Magnitude

6

ClinVar
Risk	rs869320783(-;-)
Alt	rs869320783(-;-)
Reference	Rs869320783(TT;TT)
Significance	Pathogenic
Disease	Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32913107_32913108delTT
CLNSRC
CLNACC	RCV000211039.3,