rs886038161

Merged into

rs80359638

Orientation

plus

Stabilized

plus

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

Make rs886038161(-;-)

Reference

GRCh38.p7 38.3/149

Chromosome

13

Position

32354962

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs886038161
dbSNP (classic)	rs886038161
ClinGen	rs886038161
ebi	rs886038161
HLI	rs886038161
Exac	rs886038161
Gnomad	rs886038161
Varsome	rs886038161
LitVar	rs886038161
Map	rs886038161
PheGenI	rs886038161
Biobank	rs886038161
1000 genomes	rs886038161
hgdp	rs886038161
ensembl	rs886038161
geneview	rs886038161
scholar	rs886038161
google	rs886038161
pharmgkb	rs886038161
gwascentral	rs886038161
openSNP	rs886038161
23andMe	rs886038161
SNPshot	rs886038161
SNPdbe	rs886038161
MSV3d	rs886038161
GWAS Ctlg	rs886038161

Status

Merged into rs80359638

Max Magnitude

6

ClinVar
Risk
Alt
Reference	Rs886038161(AA;AA)
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.32929099_32929100delAA
CLNSRC	Breast Cancer Information Core (BRCA2)
CLNACC	RCV000045144.2, RCV000241365.3,