SNP Detail For rs17067123
1.Mapping Information
Human SNP ID rs17067123
Human chromosome chr4
Human SNP position 179127208
Pig chromosome chr15
Pig SNP position 47485223
2.Annotation Information
PubMed ID19684573
JournalNature
Linkwww.ncbi.nlm.nih.gov/pubmed/19684573
StudyGenetic variation in IL28B predicts hepatitis C treatment-induced viral clearance.
Disease/TraitResponse to hepatitis C treatment
Initial sample871 European ancestry cases, 191 African American cases, 75 Hispanic cases
Replication sampleNA
Region4q34.3
Chromosome idchr4
Chromosome position179127208
Reported geneintergenic
Mapped geneLOC105377563 - LOC105377564
Upstream gene id105377563
Downstream gene id105377564
SNP gene ids
Upstream gene distance309882
Downstream gene distance837651
SNP risk allelers17067123-?
SNPsrs17067123
Merged0
SNP id current17067123
Contextintergenic_variant
Intergenic1
Allele frequencyNR
P value0.000008
Pvalue mlog5.09691001300805
P value text(combined)
Or beta
%95 Ci
PlatformIllumina [565759]
CNVN
Mapped traitChronic Hepatitis C infection
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0004220
Study accessionGCST000465