rs878853619

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs878853619(-;-)

Make rs878853619(-;C)

Reference

GRCh38.p2 38.2/147

Chromosome

13

Position

32394702

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs878853619
dbSNP (classic)	rs878853619
ClinGen	rs878853619
ebi	rs878853619
HLI	rs878853619
Exac	rs878853619
Gnomad	rs878853619
Varsome	rs878853619
LitVar	rs878853619
Map	rs878853619
PheGenI	rs878853619
Biobank	rs878853619
1000 genomes	rs878853619
hgdp	rs878853619
ensembl	rs878853619
geneview	rs878853619
scholar	rs878853619
google	rs878853619
pharmgkb	rs878853619
gwascentral	rs878853619
openSNP	rs878853619
23andMe	rs878853619
SNPshot	rs878853619
SNPdbe	rs878853619
MSV3d	rs878853619
GWAS Ctlg	rs878853619

Max Magnitude

0

ClinVar
Risk	rs878853619(-;-)
Alt	rs878853619(-;-)
Reference	Rs878853619(C;C)
Significance	Pathogenic
Disease	Hereditary breast and ovarian cancer syndrome
Variation	info
Gene	BRCA2
CLNDBN	Hereditary breast and ovarian cancer syndrome
Reversed	0
HGVS	NC_000013.10:g.32968839delC
CLNSRC
CLNACC	RCV000232594.1,