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

rs869320794

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs869320794(-;T)
Make rs869320794(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32339521
GeneBRCA2
is asnp
is mentioned by
dbSNPrs869320794
dbSNP (old)rs869320794
ClinGenrs869320794
ebirs869320794
HLIrs869320794
Exacrs869320794
Gnomadrs869320794
Varsomers869320794
Maprs869320794
PheGenIrs869320794
Biobankrs869320794
1000 genomesrs869320794
hgdprs869320794
ensemblrs869320794
gopubmedrs869320794
geneviewrs869320794
scholarrs869320794
googlers869320794
pharmgkbrs869320794
gwascentralrs869320794
openSNPrs869320794
23andMers869320794
23andMe allrs869320794
SNP Nexus

SNPshotrs869320794
SNPdbers869320794
MSV3drs869320794
GWAS Ctlgrs869320794
Max Magnitude0
ClinVar
Risk rs869320794(T;T)
Alt rs869320794(T;T)
Reference Rs869320794(-;-)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32913658dupT
CLNSRC
CLNACC RCV000211045.1,