rs886040499

Orientation

plus

Stabilized

plus

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

Make rs886040499(-;-)

Reference

GRCh38.p7 38.3/149

Chromosome

13

Position

32338184

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs886040499
dbSNP (classic)	rs886040499
ClinGen	rs886040499
ebi	rs886040499
HLI	rs886040499
Exac	rs886040499
Gnomad	rs886040499
Varsome	rs886040499
LitVar	rs886040499
Map	rs886040499
PheGenI	rs886040499
Biobank	rs886040499
1000 genomes	rs886040499
hgdp	rs886040499
ensembl	rs886040499
geneview	rs886040499
scholar	rs886040499
google	rs886040499
pharmgkb	rs886040499
gwascentral	rs886040499
openSNP	rs886040499
23andMe	rs886040499
SNPshot	rs886040499
SNPdbe	rs886040499
MSV3d	rs886040499
GWAS Ctlg	rs886040499

Max Magnitude

6

ClinVar
Risk	rs886040499(-;-)
Alt	rs886040499(-;-)
Reference	Rs886040499(AA;AA)
Significance	Pathogenic
Disease	Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32912321_32912322delAA
CLNSRC
CLNACC	RCV000257176.2,