rs886040792

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;GGCAA)	6	BRCA2 variant considered pathogenic for breast cancer
(AGGCA;AGGCA)	0	common in clinvar
(GGCAA;GGCAA)	0	common/normal

Make rs886040792(-;-)

Reference

GRCh38.p7 38.3/149

Chromosome

13

Position

32379360

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs886040792
dbSNP (classic)	rs886040792
ClinGen	rs886040792
ebi	rs886040792
HLI	rs886040792
Exac	rs886040792
Gnomad	rs886040792
Varsome	rs886040792
LitVar	rs886040792
Map	rs886040792
PheGenI	rs886040792
Biobank	rs886040792
1000 genomes	rs886040792
hgdp	rs886040792
ensembl	rs886040792
geneview	rs886040792
scholar	rs886040792
google	rs886040792
pharmgkb	rs886040792
gwascentral	rs886040792
openSNP	rs886040792
23andMe	rs886040792
SNPshot	rs886040792
SNPdbe	rs886040792
MSV3d	rs886040792
GWAS Ctlg	rs886040792

Max Magnitude

6

ClinVar
Risk	rs886040792(-;-)
Alt	rs886040792(-;-)
Reference	Rs886040792(AGGCA;AGGCA)
Significance	Pathogenic
Disease	Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32953497_32953501delGGCAA
CLNSRC
CLNACC	RCV000256826.2,