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rs17067123

From SNPedia

Orientationplus
Stabilizedplus
Make rs17067123(C;C)
Make rs17067123(C;T)
Make rs17067123(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position179127208
is asnp
is mentioned by
dbSNPrs17067123
ebirs17067123
HLIrs17067123
Exacrs17067123
Varsomers17067123
Maprs17067123
PheGenIrs17067123
hapmaprs17067123
1000 genomesrs17067123
hgdprs17067123
ensemblrs17067123
gopubmedrs17067123
geneviewrs17067123
scholarrs17067123
googlers17067123
pharmgkbrs17067123
gwascentralrs17067123
openSNPrs17067123
23andMers17067123
23andMe allrs17067123
SNP Nexus

SNPshotrs17067123
SNPdbers17067123
MSV3drs17067123
GWAS Ctlgrs17067123
GMAF0.2213
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19684573]
Trait Response to Hepatitis C treatment
Title Genetic variation in IL28B predicts hepatitis C treatment-induced viral clearance
Risk Allele
P-val 0.000008
Odds Ratio NR NR


GET Evidence
rs17067123
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.210938
summary