rs886038147

Merged into

rs80359587

Orientation

plus

Stabilized

plus

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

Make rs886038147(-;-)

Reference

GRCh38.p7 38.3/149

Chromosome

13

Position

32340789

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs886038147
dbSNP (classic)	rs886038147
ClinGen	rs886038147
ebi	rs886038147
HLI	rs886038147
Exac	rs886038147
Gnomad	rs886038147
Varsome	rs886038147
LitVar	rs886038147
Map	rs886038147
PheGenI	rs886038147
Biobank	rs886038147
1000 genomes	rs886038147
hgdp	rs886038147
ensembl	rs886038147
geneview	rs886038147
scholar	rs886038147
google	rs886038147
pharmgkb	rs886038147
gwascentral	rs886038147
openSNP	rs886038147
23andMe	rs886038147
SNPshot	rs886038147
SNPdbe	rs886038147
MSV3d	rs886038147
GWAS Ctlg	rs886038147

Status

Merged into rs80359587

Max Magnitude

6

ClinVar
Risk
Alt
Reference	Rs886038147(A;A)
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.32914926delA
CLNSRC	Breast Cancer Information Core (BRCA2)
CLNACC	RCV000044944.2, RCV000241168.3,