rs886038129

Merged into

rs276174862

Orientation

plus

Stabilized

plus

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

Make rs886038129(-;-)

Reference

GRCh38.p7 38.3/149

Chromosome

13

Position

32340075

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs886038129
dbSNP (classic)	rs886038129
ClinGen	rs886038129
ebi	rs886038129
HLI	rs886038129
Exac	rs886038129
Gnomad	rs886038129
Varsome	rs886038129
LitVar	rs886038129
Map	rs886038129
PheGenI	rs886038129
Biobank	rs886038129
1000 genomes	rs886038129
hgdp	rs886038129
ensembl	rs886038129
geneview	rs886038129
scholar	rs886038129
google	rs886038129
pharmgkb	rs886038129
gwascentral	rs886038129
openSNP	rs886038129
23andMe	rs886038129
SNPshot	rs886038129
SNPdbe	rs886038129
MSV3d	rs886038129
GWAS Ctlg	rs886038129

Status

Merged into rs276174862

Max Magnitude

6

ClinVar
Risk
Alt
Reference	Rs886038129(CTCT;CTCT)
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.32914212_32914215delCTCT
CLNSRC	Breast Cancer Information Core (BRCA2)
CLNACC	RCV000044727.2, RCV000241138.3,