rs869312761

Merged into

rs80359763

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(TG;TG)	0	common in clinvar

Make rs869312761(-;-)

Make rs869312761(-;TG)

Reference

GRCh38.p2 38.2/147

Chromosome

13

Position

32394866

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs869312761
dbSNP (classic)	rs869312761
ClinGen	rs869312761
ebi	rs869312761
HLI	rs869312761
Exac	rs869312761
Gnomad	rs869312761
Varsome	rs869312761
LitVar	rs869312761
Map	rs869312761
PheGenI	rs869312761
Biobank	rs869312761
1000 genomes	rs869312761
hgdp	rs869312761
ensembl	rs869312761
geneview	rs869312761
scholar	rs869312761
google	rs869312761
pharmgkb	rs869312761
gwascentral	rs869312761
openSNP	rs869312761
23andMe	rs869312761
SNPshot	rs869312761
SNPdbe	rs869312761
MSV3d	rs869312761
GWAS Ctlg	rs869312761

Status

Merged into rs80359763

Max Magnitude

0

ClinVar
Risk
Alt
Reference	Rs869312761(TG;TG)
Significance	Pathogenic
Disease	Breast-ovarian cancer Familial cancer of breast Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer not provided
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2 Familial cancer of breast Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer, familial 1 not provided
Reversed	0
HGVS	NC_000013.10:g.32969004_32969005delGT
CLNSRC	Breast Cancer Information Core (BRCA2)
CLNACC	RCV000031823.6, RCV000074563.5, RCV000131046.3, RCV000205868.1, RCV000210147.1, RCV000235145.1,