rs886038073

Merged into

rs397507284

Orientation

plus

Stabilized

plus

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

Make rs886038073(-;-)

Reference

GRCh38.p7 38.3/149

Chromosome

13

Position

32336680

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs886038073
dbSNP (classic)	rs886038073
ClinGen	rs886038073
ebi	rs886038073
HLI	rs886038073
Exac	rs886038073
Gnomad	rs886038073
Varsome	rs886038073
LitVar	rs886038073
Map	rs886038073
PheGenI	rs886038073
Biobank	rs886038073
1000 genomes	rs886038073
hgdp	rs886038073
ensembl	rs886038073
geneview	rs886038073
scholar	rs886038073
google	rs886038073
pharmgkb	rs886038073
gwascentral	rs886038073
openSNP	rs886038073
23andMe	rs886038073
SNPshot	rs886038073
SNPdbe	rs886038073
MSV3d	rs886038073
GWAS Ctlg	rs886038073

Status

Merged into rs397507284

Max Magnitude

6

ClinVar
Risk
Alt
Reference	Rs886038073(C;C)
Significance	Pathogenic
Disease	Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32910817delC
CLNSRC
CLNACC	RCV000240979.2,