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rs16885294

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs16885294(C;C)
Make rs16885294(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position54400598
is asnp
is mentioned by
dbSNPrs16885294
ebirs16885294
HLIrs16885294
Exacrs16885294
Varsomers16885294
Maprs16885294
PheGenIrs16885294
hapmaprs16885294
1000 genomesrs16885294
hgdprs16885294
ensemblrs16885294
gopubmedrs16885294
geneviewrs16885294
scholarrs16885294
googlers16885294
pharmgkbrs16885294
gwascentralrs16885294
openSNPrs16885294
23andMers16885294
23andMe allrs16885294
SNP Nexus

SNPshotrs16885294
SNPdbers16885294
MSV3drs16885294
GWAS Ctlgrs16885294
GMAF0.05969
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20923822OA-icon.png]
Trait
Title Radiation pharmacogenomics: A genome-wide association approach to identify radiation response biomarkers using human lymphoblastoid cell lines
Risk Allele
P-val 4E-7
Odds Ratio None None