rs886038152

Merged into

rs606231404

Orientation

plus

Stabilized

plus

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

Make rs886038152(-;-)

Reference

GRCh38.p7 38.3/149

Chromosome

13

Position

32341000

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs886038152
dbSNP (classic)	rs886038152
ClinGen	rs886038152
ebi	rs886038152
HLI	rs886038152
Exac	rs886038152
Gnomad	rs886038152
Varsome	rs886038152
LitVar	rs886038152
Map	rs886038152
PheGenI	rs886038152
Biobank	rs886038152
1000 genomes	rs886038152
hgdp	rs886038152
ensembl	rs886038152
geneview	rs886038152
scholar	rs886038152
google	rs886038152
pharmgkb	rs886038152
gwascentral	rs886038152
openSNP	rs886038152
23andMe	rs886038152
SNPshot	rs886038152
SNPdbe	rs886038152
MSV3d	rs886038152
GWAS Ctlg	rs886038152

Status

Merged into rs606231404

Max Magnitude

6

ClinVar
Risk
Alt
Reference	Rs886038152(ACTCC;ACTCC)
Significance	Pathogenic
Disease	Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32915137_32915141delCTCCA
CLNSRC	Breast Cancer Information Core (BRCA2)
CLNACC	RCV000241493.2,