Have questions? Visit https://www.reddit.com/r/SNPedia

rs869312761

From SNPedia

Orientationplus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs869312761(-;-)
Make rs869312761(-;TG)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32394866
GeneBRCA2
is asnp
is mentioned by
dbSNPrs869312761
ebirs869312761
HLIrs869312761
Exacrs869312761
Varsomers869312761
Maprs869312761
PheGenIrs869312761
hapmaprs869312761
1000 genomesrs869312761
hgdprs869312761
ensemblrs869312761
gopubmedrs869312761
geneviewrs869312761
scholarrs869312761
googlers869312761
pharmgkbrs869312761
gwascentralrs869312761
openSNPrs869312761
23andMers869312761
23andMe allrs869312761
SNP Nexus

SNPshotrs869312761
SNPdbers869312761
MSV3drs869312761
GWAS Ctlgrs869312761
Max Magnitude0
ClinVar
Risk rs869312761(;)
Alt rs869312761(;)
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 RCV000031823.4, RCV000074563.5, RCV000131046.2, RCV000205868.1, RCV000210147.1, RCV000235145.1,