rs886038132

Merged into

rs276174864

Orientation

plus

Stabilized

plus

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

Make rs886038132(-;-)

Reference

GRCh38.p7 38.3/149

Chromosome

13

Position

32340246

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs886038132
dbSNP (classic)	rs886038132
ClinGen	rs886038132
ebi	rs886038132
HLI	rs886038132
Exac	rs886038132
Gnomad	rs886038132
Varsome	rs886038132
LitVar	rs886038132
Map	rs886038132
PheGenI	rs886038132
Biobank	rs886038132
1000 genomes	rs886038132
hgdp	rs886038132
ensembl	rs886038132
geneview	rs886038132
scholar	rs886038132
google	rs886038132
pharmgkb	rs886038132
gwascentral	rs886038132
openSNP	rs886038132
23andMe	rs886038132
SNPshot	rs886038132
SNPdbe	rs886038132
MSV3d	rs886038132
GWAS Ctlg	rs886038132

Status

Merged into rs276174864

Max Magnitude

6

Note: this SNP is functionally equivalent to rs276174864

ClinVar
Risk
Alt
Reference	Rs886038132(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.32914383delA
CLNSRC	Breast Cancer Information Core (BRCA2)
CLNACC	RCV000044785.2, RCV000241431.2,