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

rs80358923

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs80358923(C;C)
Make rs80358923(C;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32346848
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80358923
ebirs80358923
HLIrs80358923
Exacrs80358923
Varsomers80358923
Maprs80358923
PheGenIrs80358923
hapmaprs80358923
1000 genomesrs80358923
hgdprs80358923
ensemblrs80358923
gopubmedrs80358923
geneviewrs80358923
scholarrs80358923
googlers80358923
pharmgkbrs80358923
gwascentralrs80358923
openSNPrs80358923
23andMers80358923
23andMe allrs80358923
SNP Nexus

SNPshotrs80358923
SNPdbers80358923
MSV3drs80358923
GWAS Ctlgrs80358923
Max Magnitude0
ClinVar
Risk rs80358923(A,C;A,C)
Alt rs80358923(A,C;A,C)
Reference rs80358923(T;T)
Significance Pathogenic
Disease Breast-ovarian cancer not provided Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 not provided Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32920985T>A; NC_000013.10:g.32920985T>C
CLNSRC ClinVar
CLNACC RCV000082965.2, RCV000216188.1, RCV000045098.2, RCV000113679.1,