rs863224828

Orientation

plus

Stabilized

plus

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

Make rs863224828(-;-)

Reference

GRCh38.p2 38.2/146

Chromosome

13

Position

32362663

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs863224828
dbSNP (classic)	rs863224828
ClinGen	rs863224828
ebi	rs863224828
HLI	rs863224828
Exac	rs863224828
Gnomad	rs863224828
Varsome	rs863224828
LitVar	rs863224828
Map	rs863224828
PheGenI	rs863224828
Biobank	rs863224828
1000 genomes	rs863224828
hgdp	rs863224828
ensembl	rs863224828
geneview	rs863224828
scholar	rs863224828
google	rs863224828
pharmgkb	rs863224828
gwascentral	rs863224828
openSNP	rs863224828
23andMe	rs863224828
SNPshot	rs863224828
SNPdbe	rs863224828
MSV3d	rs863224828
GWAS Ctlg	rs863224828

Max Magnitude

6

ClinVar
Risk	rs863224828(-;-)
Alt	rs863224828(-;-)
Reference	Rs863224828(C;C)
Significance	Pathogenic
Disease	Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer not provided
Variation	info
Gene	BRCA2
CLNDBN	Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer, familial 2 not provided
Reversed	0
HGVS	NC_000013.10:g.32936800delC
CLNSRC
CLNACC	RCV000196534.1, RCV000241241.1, RCV000480587.1,