rs886038069

Merged into

rs80359321

Orientation

plus

Stabilized

plus

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

Make rs886038069(-;-)

Reference

GRCh38.p7 38.3/149

Chromosome

13

Position

32336440

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs886038069
dbSNP (classic)	rs886038069
ClinGen	rs886038069
ebi	rs886038069
HLI	rs886038069
Exac	rs886038069
Gnomad	rs886038069
Varsome	rs886038069
LitVar	rs886038069
Map	rs886038069
PheGenI	rs886038069
Biobank	rs886038069
1000 genomes	rs886038069
hgdp	rs886038069
ensembl	rs886038069
geneview	rs886038069
scholar	rs886038069
google	rs886038069
pharmgkb	rs886038069
gwascentral	rs886038069
openSNP	rs886038069
23andMe	rs886038069
SNPshot	rs886038069
SNPdbe	rs886038069
MSV3d	rs886038069
GWAS Ctlg	rs886038069

Status

Merged into rs80359321

Max Magnitude

6

ClinVar
Risk
Alt
Reference	Rs886038069(AAGGA;AAGGA)
Significance	Pathogenic
Disease	Familial cancer of breast Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32910577_32910581delGGAAA
CLNSRC	Breast Cancer Information Core (BRCA2)
CLNACC	RCV000043941.2, RCV000241255.2,