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

rs11177074

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs11177074(C;C)
Make rs11177074(C;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position68150654
is asnp
is mentioned by
dbSNPrs11177074
ebirs11177074
HLIrs11177074
Exacrs11177074
Varsomers11177074
Maprs11177074
PheGenIrs11177074
hapmaprs11177074
1000 genomesrs11177074
hgdprs11177074
ensemblrs11177074
gopubmedrs11177074
geneviewrs11177074
scholarrs11177074
googlers11177074
pharmgkbrs11177074
gwascentralrs11177074
openSNPrs11177074
23andMers11177074
23andMe allrs11177074
SNP Nexus

SNPshotrs11177074
SNPdbers11177074
MSV3drs11177074
GWAS Ctlgrs11177074
GMAF0.1028
Max Magnitude0
? (C;C) (C;T) (T;T) 28
[PMID 20084279OA-icon.png] Common Genetic Variants and Risk for HPV Persistence and Progression to Cervical Cancer