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rs2894054

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs2894054(C;T)
Make rs2894054(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position30904497
is asnp
is mentioned by
dbSNPrs2894054
ebirs2894054
HLIrs2894054
Exacrs2894054
Varsomers2894054
Maprs2894054
PheGenIrs2894054
hapmaprs2894054
1000 genomesrs2894054
hgdprs2894054
ensemblrs2894054
gopubmedrs2894054
geneviewrs2894054
scholarrs2894054
googlers2894054
pharmgkbrs2894054
gwascentralrs2894054
openSNPrs2894054
23andMers2894054
23andMe allrs2894054
SNP Nexus

SNPshotrs2894054
SNPdbers2894054
MSV3drs2894054
GWAS Ctlgrs2894054
GMAF0.1084
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