rs886038142

Merged into

rs80359569

Orientation

plus

Stabilized

plus

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

Make rs886038142(-;-)

Reference

GRCh38.p7 38.3/149

Chromosome

13

Position

32340594

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs886038142
dbSNP (classic)	rs886038142
ClinGen	rs886038142
ebi	rs886038142
HLI	rs886038142
Exac	rs886038142
Gnomad	rs886038142
Varsome	rs886038142
LitVar	rs886038142
Map	rs886038142
PheGenI	rs886038142
Biobank	rs886038142
1000 genomes	rs886038142
hgdp	rs886038142
ensembl	rs886038142
geneview	rs886038142
scholar	rs886038142
google	rs886038142
pharmgkb	rs886038142
gwascentral	rs886038142
openSNP	rs886038142
23andMe	rs886038142
SNPshot	rs886038142
SNPdbe	rs886038142
MSV3d	rs886038142
GWAS Ctlg	rs886038142

Status

Merged into rs80359569

Max Magnitude

6

ClinVar
Risk
Alt
Reference	Rs886038142(T;T)
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.32914731delT
CLNSRC	Breast Cancer Information Core (BRCA2)
CLNACC	RCV000044877.2, RCV000241032.2,