rs886040519

Orientation

plus

Stabilized

plus

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

Make rs886040519(C;C)

Reference

GRCh38.p7 38.3/149

Chromosome

13

Position

32326103

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs886040519
dbSNP (classic)	rs886040519
ClinGen	rs886040519
ebi	rs886040519
HLI	rs886040519
Exac	rs886040519
Gnomad	rs886040519
Varsome	rs886040519
LitVar	rs886040519
Map	rs886040519
PheGenI	rs886040519
Biobank	rs886040519
1000 genomes	rs886040519
hgdp	rs886040519
ensembl	rs886040519
geneview	rs886040519
scholar	rs886040519
google	rs886040519
pharmgkb	rs886040519
gwascentral	rs886040519
openSNP	rs886040519
23andMe	rs886040519
SNPshot	rs886040519
SNPdbe	rs886040519
MSV3d	rs886040519
GWAS Ctlg	rs886040519

Max Magnitude

6

ClinVar
Risk	rs886040519(C;C)
Alt	rs886040519(C;C)
Reference	Rs886040519(-;-)
Significance	Pathogenic
Disease	Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32900240dupC
CLNSRC
CLNACC	RCV000257101.2,